OntologiesCurators at RGD make annotations to genes, QTLs and strains using standardized vocabularies/ontologies. Your search returned annotations to the terms below.ChEBI: ChEBI Ontology
(-)-beta-caryophyllene
(-)-menthol
(11)C-modified compound
(1R)-primary fluorescent chlorophyll catabolite
(1S)-primary fluorescent chlorophyll catabolite
(2E,4E)-hexa-2,4-dienoic acid
(3aS,4R,9bR)-golgicide A
(E)-1-hydroxy-2-(non-1-en-1-yl)quinolin-4-one
(R)-mosapramine
(R)-mosapride
(S)-mosapramine
(S)-mosapride
(S)-nicotine
1-(4-bromophenyl)-2-phenylethan-1-one
1-adamantanecarboxylic acid [2-(2-furanylmethylamino)-2-oxoethyl] ester
1-ethyl-N-[3-(4-morpholinyl)propyl]-2-oxo-6-benzo[cd]indolesulfonamide
1-phenyl-N-(3-propan-2-yloxypropyl)-4-pyrazolo[3,4-d]pyrimidinamine
15-acetyldeoxynivalenol
2'-fucosyllactose
2,4-dinitrotoluene
2-amino-4-(\{1-[(carboxymethyl)-C-hydroxycarbonimidoyl]-2-(\{4,10,11,14,16-pentahydroxy-5,9,11,13,13-pentamethyl-2-[1-(2-methyl-1,3-thiazol-4-yl)prop-1-en-2-yl]-12-oxo-1-azacyclohexadec-1(16)-en-5-yl\}sulfanyl)ethyl\}-C-hydroxycarbonimidoyl)butanoic acid
2-chloro-4-nitrotoluene
3,3',5-triiodo-L-thyronine
3,4-dinitrotoluene
3-acetyldeoxynivalenol
4-[(Z)-[1-(3-Nitrophenyl)-5-oxo-3-phenylpyrazol-4-ylidene]methyl]benzoic acid
4-chloro-3,5-dimethylphenol
6-O-methylguanine
6alpha-Hydroxy-3-oxo-5beta-cholan-24-oic Acid
[4)-beta-D-GlcpA-(1->4)-alpha-D-GlcpNAc6OS-(1->]n
[4)-beta-D-GlcpA-(1->4)-alpha-D-GlcpNS6OS-(1->]n
A. baumannii strain 54149 exopolysaccharide
acetaldehyde
actinomycin X2
albumin type
alkaloid
all-cis-docosa-7,10,13,16-tetraenoic acid
allomelanin
alpha-methylnoradrenaline
alternariol
aristolochic acid A
arsenopyrite
bafilomycin A1
barium sulfate
bentonite
beta-alanine betaine
beta-amyrin
beta-carotene
beta-caryophyllene
beta-Gal-(1->3)-beta-GalNAc-(1->4)-[alpha-Neu5Ac-(2->8)-alpha-Neu5Ac-(2->3)]-beta-Gal-(1->4)-beta-Glc-(1<->1')-Cer 1(II''),9(II')-lactone
bioallethrin
bitertanol
bryostatin 1
butopamine
cacibiocin A
cantharidin
carbohydrate
carboxylic acid
carrageenan
CDP-diacylglycerol
ceforanide
cephalosporin
cephapirin sodium
Cer(d16:1(4E)(1OH,3OH)(15Me)/21:0(2OH[R]))
chalcopyrite
chlorotoluron
chloroxuron
CID 91850115
cinchocaine
cinchonidine
cinchonine
cis-fatty acid
cis-golgicide A
colistin
Crenigacestat
cyazofamid
cyprodinil
difenoconazole
dinitrogen oxide
dinocap
dinocap-6
dioxo(sulfanyl)molybdenum
dipolar compound
diquat
djalonensone
dopamine uptake inhibitor
drotaverine
echinocandin
elemental cadmium
epoxiconazole
epoxyazadiradione
ethaboxam
fenticlor
feselol
fluorotelomer alcohol
fluoxytioconazole (thiol)
gallotannin
gamma-terpinene
glyceryl monothioglycolate
glycol ether
glyphosate
golgicide A
haematoxylin
haloxyfop
haloxyfop-P
haloxyfop-P-methyl
helium-4 atom
heme b
huperzine A
insulin
iron(2+) sulfate (anhydrous)
isocyanic acid
ivermectin
juvenile hormone III
kadethrin
Kaempferol 3-(2''-galloyl-alpha-L-arabinopyranoside)
LAC dye
lactose
lichenin
low-density lipoprotein
LPIM1(18:0/0:0)
lupanine
lycojapodine A
malathion
mannoprotein
maytansinoid
melanins
metaldehyde
metam
methallatal
methylparaben
mianserin
microcystin
microcystin-LR
molybdenum disulfide
molybdenum disulfide nanotube
morphine
mosapramine
mosapramine dihydrochloride
mosapride
mosapride citrate dihydrate
Moschamindole
moscovium atom
moscovium molecular entity
Mosesin 4
Mosin C
Mosinone A
Mosloflavone
mucilage
N(2)-([biphenyl]-4-ylsulfonyl)-N-hydroxy-N(2)-isopropoxy-D-valinamide
N,N-diethyl-m-toluamide
N-(2,6-difluorophenyl)-5-[3-[2-[5-ethyl-2-methoxy-4-[4-(4-methylsulfonyl-1-piperazinyl)-1-piperidinyl]anilino]-4-pyrimidinyl]-2-imidazo[1,2-a]pyridinyl]-2-methoxybenzamide
N-(2-hydroxyhenicosanoyl)-15-methylhexadecasphing-4-enine
N-(3-\{[alpha-D-GalN-(1->4)-alpha-D-GalN-(1->4)-alpha-D-GalN-(1->4)-alpha-D-GalN-(1->4)-alpha-D-GalN-(1->4)-alpha-D-GalN-yl]oxy\}propyl)-21-(biotinylamino)-4,7,10,13,16,19-hexaoxadodecan-1-amide
N-(3-\{[alpha-D-GalN-(1->4)-alpha-D-GalN-(1->4)-alpha-D-GalN-(1->4)-alpha-D-GalN-(1->4)-alpha-D-GalN-yl]oxy\}propyl)-21-(biotinylamino)-4,7,10,13,16,19-hexaoxadodecan-1-amide
N-(3-\{[alpha-D-GalN-(1->4)-alpha-D-GalN-(1->4)-alpha-D-GalN-(1->4)-alpha-D-GalN-yl]oxy\}propyl)-21-(biotinylamino)-4,7,10,13,16,19-hexaoxadodecan-1-amide
N-(3-\{[alpha-D-GalN-(1->4)-alpha-D-GalN-(1->4)-alpha-D-GalN-yl]oxy\}propyl)-21-(biotinylamino)-4,7,10,13,16,19-hexaoxadodecan-1-amide
N-(3-\{[alpha-D-GalN-(1->4)-alpha-D-GalN-yl]oxy\}propyl)-21-(biotinylamino)-4,7,10,13,16,19-hexaoxadodecan-1-amide
N-(3-\{[alpha-D-GalNAc-(1->4)-alpha-D-GalNAc-(1->4)-alpha-D-GalNAc-(1->4)-alpha-D-GalNAc-(1->4)-alpha-D-GalNAc-(1->4)-alpha-D-GalNAc-yl]oxy\}propyl)-21-(biotinylamino)-4,7,10,13,16,19-hexaoxadodecan-1-amide
N-(3-\{[alpha-D-GalNAc-(1->4)-alpha-D-GalNAc-(1->4)-alpha-D-GalNAc-(1->4)-alpha-D-GalNAc-(1->4)-alpha-D-GalNAc-yl]oxy\}propyl)-21-(biotinylamino)-4,7,10,13,16,19-hexaoxadodecan-1-amide
N-(3-\{[alpha-D-GalNAc-(1->4)-alpha-D-GalNAc-(1->4)-alpha-D-GalNAc-(1->4)-alpha-D-GalNAc-yl]oxy\}propyl)-21-(biotinylamino)-4,7,10,13,16,19-hexaoxadodecan-1-amide
N-(3-\{[alpha-D-GalNAc-(1->4)-alpha-D-GalNAc-(1->4)-alpha-D-GalNAc-yl]oxy\}propyl)-21-(biotinylamino)-4,7,10,13,16,19-hexaoxadodecan-1-amide
N-(3-\{[alpha-D-GalNAc-(1->4)-alpha-D-GalNAc-yl]oxy\}propyl)-21-(biotinylamino)-4,7,10,13,16,19-hexaoxadodecan-1-amide
N-[(3R,9R,10R)-9-[[cyclohexylmethyl(methyl)amino]methyl]-12-[(2R)-1-hydroxypropan-2-yl]-3,10-dimethyl-13-oxo-2,8-dioxa-12-azabicyclo[12.4.0]octadeca-1(14),15,17-trien-16-yl]methanesulfonamide
N-[(3R,9R,10R)-9-[[cyclohexylmethyl(methyl)amino]methyl]-12-[(2S)-1-hydroxypropan-2-yl]-3,10-dimethyl-13-oxo-2,8-dioxa-12-azabicyclo[12.4.0]octadeca-1(14),15,17-trien-16-yl]methanesulfonamide
N-[(3R,9R,10S)-9-[[cyclohexylmethyl(methyl)amino]methyl]-12-[(2R)-1-hydroxypropan-2-yl]-3,10-dimethyl-13-oxo-2,8-dioxa-12-azabicyclo[12.4.0]octadeca-1(14),15,17-trien-16-yl]methanesulfonamide
N-[(3R,9R,10S)-9-[[cyclohexylmethyl(methyl)amino]methyl]-12-[(2S)-1-hydroxypropan-2-yl]-3,10-dimethyl-13-oxo-2,8-dioxa-12-azabicyclo[12.4.0]octadeca-1(14),15,17-trien-16-yl]methanesulfonamide
N-[(3R,9S,10R)-9-[[cyclohexylmethyl(methyl)amino]methyl]-12-[(2R)-1-hydroxypropan-2-yl]-3,10-dimethyl-13-oxo-2,8-dioxa-12-azabicyclo[12.4.0]octadeca-1(14),15,17-trien-16-yl]methanesulfonamide
N-[(3R,9S,10R)-9-[[cyclohexylmethyl(methyl)amino]methyl]-12-[(2S)-1-hydroxypropan-2-yl]-3,10-dimethyl-13-oxo-2,8-dioxa-12-azabicyclo[12.4.0]octadeca-1(14),15,17-trien-16-yl]methanesulfonamide
N-[(3R,9S,10S)-9-[[cyclohexylmethyl(methyl)amino]methyl]-12-[(2R)-1-hydroxypropan-2-yl]-3,10-dimethyl-13-oxo-2,8-dioxa-12-azabicyclo[12.4.0]octadeca-1(14),15,17-trien-16-yl]methanesulfonamide
N-[(3S,9R,10S)-9-[[cyclohexylmethyl(methyl)amino]methyl]-12-[(2R)-1-hydroxypropan-2-yl]-3,10-dimethyl-13-oxo-2,8-dioxa-12-azabicyclo[12.4.0]octadeca-1(14),15,17-trien-16-yl]methanesulfonamide
N-[(3S,9R,10S)-9-[[cyclohexylmethyl(methyl)amino]methyl]-12-[(2S)-1-hydroxypropan-2-yl]-3,10-dimethyl-13-oxo-2,8-dioxa-12-azabicyclo[12.4.0]octadeca-1(14),15,17-trien-16-yl]methanesulfonamide
N-[(3S,9S,10R)-9-[[cyclohexylmethyl(methyl)amino]methyl]-12-[(2R)-1-hydroxypropan-2-yl]-3,10-dimethyl-13-oxo-2,8-dioxa-12-azabicyclo[12.4.0]octadeca-1(14),15,17-trien-16-yl]methanesulfonamide
N-[(3S,9S,10R)-9-[[cyclohexylmethyl(methyl)amino]methyl]-12-[(2S)-1-hydroxypropan-2-yl]-3,10-dimethyl-13-oxo-2,8-dioxa-12-azabicyclo[12.4.0]octadeca-1(14),15,17-trien-16-yl]methanesulfonamide
N-[(3S,9S,10S)-9-[[cyclohexylmethyl(methyl)amino]methyl]-12-[(2R)-1-hydroxypropan-2-yl]-3,10-dimethyl-13-oxo-2,8-dioxa-12-azabicyclo[12.4.0]octadeca-1(14),15,17-trien-16-yl]methanesulfonamide
N-[(3S,9S,10S)-9-[[cyclohexylmethyl(methyl)amino]methyl]-12-[(2S)-1-hydroxypropan-2-yl]-3,10-dimethyl-13-oxo-2,8-dioxa-12-azabicyclo[12.4.0]octadeca-1(14),15,17-trien-16-yl]methanesulfonamide
N-[(Z)-2-[acetyl-(2-oxo-3-phenylpropyl)amino]-3-(7-methoxy-1,3-benzodioxol-5-yl)prop-1-enyl]acetamide
N-feruloylserotonin
nabumetone
NCS172285
Neoechinulin C
nitrogen-14 atom
nitroso compound
norfloxacin
ochratoxin A
oleocanthal
oleuropein
oleuropein aglycone
opine
orcein
oxygen-16 atom
palytoxin
pencycuron
pendimethalin
pentaerythritol tetranitrate
PhIP
phosphine oxide
picrocrocin
PLX5622
pramipexole(2+)
prostaglandin E2
quassinoid
quercetin
ractopamine
royal jelly
S. flexneri serotype 1a O-polysaccharide (O factor 9-positive)
S. flexneri serotype 1b O-polysaccharide (O factor 9-positive)
S. flexneri serotype 2a O-polysaccharide (O factor 9-positive)
S. flexneri serotype 5a O-polysaccharide (O factor 9-positive)
S. flexneri serotype 6 O-polysaccharide (O factor 9-positive)
S. flexneri serotype Y O-polysaccharide (O factor 9-positive)
silicon-28 atom
spiropidion
starch
sulfaguanidine
sulfur hexafluoride
sulfur-32 atom
surfactin
tetradecanoic acid
tetrahydroxy-1,4-benzoquinone hydrate
tetrathiomolybdate(2-)
thallium-205
thermorubin A
thiamine(1+) triphosphate
toxaphene
trans-beta-farnesene
trans-cis-nepetalactone
trans-golgicide A
trichothecene
undecanoic acid
vasopressin
xyloglucan
xylose
zeaxanthin bis(beta-D-glucoside)
zinc-65 atom
CL: Cell Ontology
adipocyte
alpha1-tanycyte
alpha2-tanycyte
astrocyte
basal cell of prostate epithelium
basal cell of urothelium
beta1-tanycyte
beta2-tanycyte
bone cell
candelabrum cell
capillary endothelial cell
cardiac muscle cell
CD8-alpha alpha positive, gamma-delta intraepithelial T cell
central nervous system macrophage
cerebellar Golgi cell
cerebellar granule cell
cerebral cortex endothelial cell
cerebral cortex neuron
corneal endothelial cell
corticothalamic VAL/VM projecting glutamatergic neuron of the primary motor cortex
corticothalamic-projecting glutamatergic cortical neuron
decidual natural killer cell, human
diffuse bipolar 3a cell
diffuse bipolar 3b cell
enteroglial cell
epidermal cell
epithelial cell of nephron
epithelial cell of sweat gland
erythroid progenitor cell, mammalian
fenestrated endothelial cell
fibroblast of connective tissue of nonglandular part of prostate
flat midget bipolar cell
forebrain radial glial cell
gamete
gamma-delta intraepithelial T cell
glial cell
glioblast
goblet cell
granule cell
granulosa cell
hypendymal cell
intermediate monocyte
interneuron
interstitial cell
intestinal tuft cell
intestinal villus capillary endothelial cell
intraepithelial lymphocyte
invaginating midget bipolar cell
ionocyte
kidney proximal convoluted tubule epithelial cell
L2/3 bipolar VIP GABAergic interneuron (Mmus)
L2/3-6 intratelencephalic projecting glutamatergic neuron
L5 non-Martinotti sst GABAergic interneuron (Mmus)
L5 VIP GABAergic interneuron (Mmus)
L6 th sst GABAergic interneuron (Mmus)
L6b glutamatergic cortical neuron
lens epithelial cell
Leydig cell
mast cell
mature gamma-delta T cell
megakaryocyte-erythroid progenitor cell
meis2 expressing cortical GABAergic cell
mesodermal cell
myeloblast
myelocyte
myocardial endocrine cell
myofibroblast cell
neutrophil
pancreatic acinar cell
pancreatic ductal cell
pancreatic epsilon cell
paneth cell
phagocyte
pigmented ciliary epithelial cell
pituicyte
primary cultured cell
Purkinje cell
Schwann cell
SCN pacemaker neuron
skeletal muscle satellite cell
sst GABAergic interneuron
subcutaneous adipocyte
telocyte
thermoreceptor cell
tissue-resident macrophage
type G enteroendocrine cell
type II vestibular sensory cell
urothelial cell
CMO: Clinical Measurement
anterior cerebral artery inner diameter
beta cell area to total pancreatic islet area ratio
blood beta-2 microglobulin
blood ceruloplasmin level
blood cystatin C level
blood globulin measurement
blood immunoglobulin A level
blood immunoglobulin G level
blood osteocalcin level
blood RT6.1 positive cell count to total lymphocyte count ratio
blood tissue inhibitor of metalloproteinase-1 level
blood vasopressin level
blood vitamin level
bone area measurement
bone biomechanical measurement
bone cross-sectional area measurement
bone marrow measurement
bone marrow morphological measurement
bone measurement
bone mineral content
bone mineral density
bone morphological measurement
bone physiological measurement
bone polar moment of inertia
bone polar moment of inertia to body weight ratio
bone stiffness
bone total energy absorbed before break
bone trabecular cross-sectional area
bone ultimate force
calculated bone cross-sectional area measurement
calculated bone mineral content measurement
calculated bone mineral density measurement
calculated pancreatic islet beta cell area
CD4+CD8+ thymocyte count
CD4+CD8- thymocyte count
CD4-CD8+ thymocyte count
compact volumetric bone mineral density
ERG oscillatory potential
femoral neck biomechanical measurement
femoral neck polar moment of inertia
femoral neck ultimate force
femur biomechanical measurement
femur midshaft biomechanical measurement
femur midshaft polar moment of inertia
femur polar moment of inertia
femur stiffness
femur total energy absorbed before break
femur ultimate force
forebrain ribonucleic acid level
front foot morphological measurement
front foot phalanges count
gastrocnemius ribonucleic acid level
head morphological measurement
hind foot morphological measurement
hind foot phalanges count
larynx molecular composition measurement
larynx morphological measurement
mesenteric artery ribonucleic acid level
milk beta carotene content
pancreatic islet beta cell area
plasma immunoglobulin A level
plasma immunoglobulin G level
plasma osteocalcin level
plasma vasopressin level
red blood cell count
serum beta-2 microglobulin
serum immunoglobulin A level
serum immunoglobulin G level
serum immunoglobulin G subclass level
serum immunoglobulin G1 level
serum immunoglobulin G2a level
serum osteocalcin level
serum tissue inhibitor of metalloproteinase 1 level
serum vasopressin level
spinal cord beta-2 microglobulin mRNA level
spinal cord beta-2 microglobulin protein level
substantia nigra ribonucleic acid level
telencephalon ribonucleic acid level
tibia stiffness
tibia total energy absorbed before break
tibia ultimate force
total volumetric bone mineral density
trabecular volumetric bone mineral density
urethra measurement
urethra molecular composition measurement
urethra morphological measurement
vertebra biomechanical measurement
vertebra ultimate force
volumetric bone mineral density
whole body physiology measurement
EFO: Experimental Factor Ontology
16q24.1 microdeletion syndrome
17q21.31 microduplication syndrome
3,3',5-triiodo-L-thyronine
3-hydroxy-3-methylglutaryl-CoA synthase deficiency
3C syndrome
45,X/46,XY mixed gonadal dysgenesis
4C
5-HIAA measurement
Abdominal colic
abdominal cystic lymphangioma
abdominal fibromatosis
Abnormal cartilage collagen
acetaldehyde
achondroplasia
achromatopsia 2
acquired rippling muscle disease
acquired thrombotic thrombocytopenic purpura
acral lentiginous melanoma
Acrodynia
acromesomelic dysplasia 2C, Hunter-Thompson type
acropectororenal dysplasia
actinic keratosis
Acute hepatic porphyria
acute intermittent porphyria
acute monocytic leukemia
acute proliferative glomerulonephritis
acute salpingitis
adamantinoma
adenoid cystic carcinoma
Adenomatoid Odontogenic Tumor
adenosine kinase deficiency
adipocyte
adiponectin
adiponectin (human)
adult hepatocellular carcinoma
advanced heart failure
age-related hearing impairment
alcohol sensitivity, acute
aldosterone-producing adenoma with seizures and neurological abnormalities
Alexander disease type I
alobar holoprosencephaly
Alopecia universalis
alopecia universalis congenita
alopecia-epilepsy-pyorrhea-intellectual disability syndrome
alpha-carotene measurement
Alphavirus infectious disease
altitude sickness
alveolar soft part sarcoma
ameloblastoma
anal Paget disease
anaplastic astrocytoma
anaplastic ependymoma
anencephaly 1
angiomyolipoma
angiosarcoma
angiosarcoma of the scalp
anorexia nervosa
anotia
antenna
anterior lateral line system
anterior midgut primordium
anti-NMDA receptor encephalitis
antiphospholipid syndrome
apocrine adenocarcinoma
arachnoid cyst
argininosuccinic aciduria
aristolochic acid A
Ascher syndrome
aseptic meningitis
aspergillosis
astroblastoma
astrocyte
Ataxia-oculomotor apraxia type 4
atresia of small intestine
Atrial septal defect - atrioventricular conduction defects
atrial septal defect 7
atrophic macular degeneration
attention deficit hyperactivity disorder
atypical coarctation of aorta
autosomal dominant Alport syndrome
Autosomal dominant cerebellar ataxia type 3
autosomal dominant cerebellar ataxia type III
Autosomal dominant Charcot-Marie-Tooth disease type 2B
Autosomal dominant Charcot-Marie-Tooth disease type 2J
autosomal dominant intermediate Charcot-Marie-Tooth disease type G
autosomal dominant optic atrophy, classic form
autosomal recessive Alport syndrome
autosomal recessive cerebellar ataxia
autosomal recessive congenital ichthyosis 4B
autosomal recessive limb-girdle muscular dystrophy type 2A
autosomal recessive limb-girdle muscular dystrophy type 2E
autosomal recessive limb-girdle muscular dystrophy type 2J
autosomal recessive limb-girdle muscular dystrophy type 2L
Autosomal recessive spastic paraplegia type 76
autosomal recessive transient neonatal diabetes mellitus
avascular necrosis
B-cell non-Hodgkins lymphoma
bacterial urinary tract infection
bacterial vaginosis
bacteriemia
Bamforth-Lazarus syndrome
BAP1-related tumor predisposition syndrome
Barrett's esophagus
basal cell neoplasm
basal-like breast carcinoma
basicranium
Beare-Stevenson cutis gyrata syndrome
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11
benign infantile seizures associated with mild gastroenteritis
benign lipomatous neoplasm
benign metastasizing leiomyoma
benign partial epilepsy of infancy with complex partial seizures
benign prostatic hyperplasia
benign recurrent intrahepatic cholestasis type 1
beriberi
biceps brachii
bilateral generalized polymicrogyria
bilateral renal agenesis
biliary system
Bladder Small Cell Neuroendocrine Carcinoma
Bladder Squamous Cell Carcinoma
bladder transitional cell carcinoma
bladder urachal carcinoma
Blastocystis hominis infectious disease
blood group
blue nevus
bone osteosarcoma
Bothnia retinal dystrophy
brachydactylous dwarfism, Mseleni type
Brachydactyly - arterial hypertension
brachydactyly-arterial hypertension syndrome
brachydactyly-mesomelia-intellectual disability-heart defects syndrome
brain
brain aneurysm
brain hypoxia
branchiostegal ray 1
branchiostegal ray 2
branchiostegal ray 3
Breast Diffuse Large B-Cell Lymphoma
breast ductal carcinoma in situ
breast invasive ductal carcinoma cell
breast lymphoma
breast neuroendocrine neoplasm
bringing up phlegm, sputum or mucus on most days, self-reported
Brodmann (1909) area 38
Brodmann (1909) area 46
bronchiectasis
bronchogenic cyst
Brown-Sequard Syndrome
brucellosis
bullous pemphigoid
Burkitt lymphoma cell
Buruli ulcer disease
CA2 field of hippocampus
CA3 field of hippocampus
CA4 field of hippocampus
CACNA1A-related complex neurodevelopmental disorder
calcifying epithelial odontogenic tumor
camptodactyly syndrome, Guadalajara type 2
cancer
Candidiasis, Invasive
cantharidin
capillary endothelial cell
capillary infantile hemangioma
capitellum
carbamoyl phosphate synthetase I deficiency disease
carbohydrate
carboxylic acid
carbuncle
carcinoma
carcinoma ex pleomorphic adenoma
carcinoma of gallbladder and extrahepatic biliary tract
cardiac muscle cell
cardioacrofacial dysplasia 2
cardiofaciocutaneous syndrome
carnitine palmitoyl transferase II deficiency, myopathic form
carotid body paraganglioma
cartilage
cartilage thickness measurement
cat-eye syndrome
cataract
cauda equina
caudal fin
CBA/J
CD8-alpha alpha positive, gamma-delta intraepithelial T cell
central nervous system macrophage
central nervous system venous angioma
central neurocytoma
cerebellar astrocytoma
cerebellar hemangioblastoma
cerebellar hemisphere
cerebellar pilocytic astrocytoma
cervical dystonia
Cervical Mucinous Adenocarcinoma, Minimal Deviation Variant
cervical squamous cell carcinoma
cervix endometriosis
Chagas cardiomyopathy
Chandler syndrome
Charcot-Marie-Tooth disease recessive intermediate C
Charcot-Marie-Tooth disease type 1B
Charcot-Marie-Tooth disease type 2B
Charcot-Marie-Tooth disease type 2J
childhood absence epilepsy
childhood brain stem glioma
cholestasis, intrahepatic, of pregnancy 3
chondroblastoma
chondromyxoid fibroma
chondrosarcoma
choriocarcinoma
chorioretinitis
choroid cancer
chromoblastomycosis
chromophobe renal cell carcinoma
chromosome 16 trisomy
chromosome 16p13.3 duplication syndrome
chromosome 17q21.31 duplication syndrome
chromosome 18 mosaic monosomy
chromosome 1q deletion
chromosome 20 trisomy
chromosome 22, monosome mosaic
chromosome 8-derived supernumerary ring/marker
chronic bronchitis
chronic kidney disease
chronic lymphocytic leukemia
chronic myelogenous leukemia
chronic periodontitis
chronic pulmonary heart disease
ciliary marginal zone
classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
classic maple syrup urine disease
classic medulloblastoma
Classical progressive supranuclear palsy
clubfoot
cognitive behavioural therapy
cold urticaria
coloboma of choroid and retina
colon
colorectal adenocarcinoma
combined oxidative phosphorylation defect type 15
complex regional pain syndrome
congenital absence of both forearm and hand
congenital bile acid synthesis defect 1
Congenital bile acid synthesis defect type 1
congenital chylothorax
congenital cornea plana
congenital dyserythropoietic anemia type 2
Congenital dyserythropoietic anemia type II
congenital esophageal diverticulum
congenital factor XIII deficiency
congenital isolated hyperinsulinism
congenital lipoid adrenal hyperplasia due to STAR deficency
congenital myopathy with cores
congenital myopathy with internal nuclei and atypical cores
congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
congenital smooth muscle hamartoma
Conjunctival Squamous Cell Carcinoma
conventional osteosarcoma
Cooper-Jabs syndrome
cornea plana
coronary aneurysm
craniofrontonasal syndrome
Craniopharyngioma
craniorachischisis
creatine biosynthetic process
Crigler-Najjar syndrome type 1
Crohn's disease
CSF-1/PDGF receptor-type tyrosine-protein kinase
Curry-Jones syndrome
Cushing syndrome due to macronodular adrenal hyperplasia
cutaneous Leishmaniasis
cutaneous mastocytosis
cutaneous nodular amyloidosis
cutaneous squamous cell carcinoma
cyclosporiasis
cystic leukoencephalopathy without megalencephaly
cytomegalovirus pneumonia
d-bifunctional protein deficiency
decidual natural killer cell, human
dedifferentiated liposarcoma
deep seated dermatophytosis
dehydroepiandrosterone sulphate measurement
Delayed ability to stand
Delayed ability to walk
deletion 5q35
dengue disease
dental caries
desmoplastic/nodular medulloblastoma
developmental and epileptic encephalopathy, 9
developmental delay and seizures with or without movement abnormalities
developmental delay with variable intellectual impairment and behavioral abnormalities
Developmental delay with variable intellectual impairment and behavioural abnormalities
Dextrotransposition of the great arteries
diabetic cardiomyopathy
diaphragmatic defect-limb deficiency-skull defect syndrome
diffuse large B-cell lymphoma
diffuse lymphatic malformation
diffuse palmoplantar keratoderma
digestive duplication cyst of the tongue
digitotalar dysmorphism
dipetalonemiasis
diquat
discitis
discoid lupus erythematosus
Disseminated Peritoneal Leiomyomatosis
disseminated superficial actinic porokeratosis
dissociation measurement
distal trisomy 20q
distal trisomy 6p
distal trisomy 9q
Down syndrome
drug-Induced dyskinesia
Duane retraction syndrome 3 with or without deafness
ductus arteriosus
duplication/inversion 15q11
Dupuytren Contracture
dysgerminoma
dyskinesia with orofacial involvement, autosomal dominant
dysplasia epiphysealis hemimelica
Dystrophic epidermolysis bullosa
early-onset generalized dystonia
early-onset non-syndromic cataract
Eastern equine encephalitis
eccrine acrospiroma
ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies
ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome
ectomesenchymoma
ectopterygoid bone
Ehlers-Danlos syndrome, hypermobility type
Ehlers-Danlos syndrome, vascular type
embryonic primordium of adult eye
encephalocraniocutaneous lipomatosis
encephalomalacia
endocervical adenocarcinoma
endocrine tuberculosis
endodermal sinus tumor
endometrial carcinoma
Endometrial Endometrioid Adenocarcinoma
endometriosis
endometrium adenocarcinoma
endomyocardial fibrosis
Enterococcus faecalis infection
enterocolitis
enteropathy-associated T-cell lymphoma
enthesitis-related juvenile idiopathic arthritis
enzootic pneumonia of calves
eosinophilic pneumonia
ependymoma
epidermal cell
Epidermal Inclusion Cyst
epidermolysis bullosa
epidermolysis bullosa acquisita
epidural neoplasm
epiglottitis
epilepsia partialis continua
epilepsy, hearing loss, and intellectual disability syndrome
Epiphyses, Slipped
epithalamus
epithelioid sarcoma
Epstein-Barr virus-positive diffuse large B-cell lymphoma of the elderly
erythema multiforme
erythema palmare hereditarium
esophageal atresia/tracheoesophageal fistula
esophageal duplication cyst
esophagus leiomyoma
essential tremor
euthyroid sick syndrome
Ewing sarcoma
Ewing sarcoma/peripheral primitive neuroectodermal tumor
Ewing sarcoma/peripheral primitive neuroectodermal tumor of bone
exercise test
exfoliation syndrome
exfoliative ichthyosis
exstrophy-epispadias complex
Extraskeletal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor
extraskeletal myxoid chondrosarcoma
familial colorectal cancer
familial Dupuytren contracture
familial focal epilepsy with variable foci
familial monosomy 7 syndrome
familial multiple nevi flammei
Familial paroxysmal ataxia
familial partial lipodystrophy
familial pityriasis rubra pilaris
familial renal glucosuria
familial rhabdoid tumor
Febrile seizure (within the age range of 3 months to 6 years)
Feingold syndrome
female breast carcinoma
fertilized egg stage
fetal and neonatal alloimmune thrombocytopenia
fg syndrome
Fibroadenoma
fibroepithelial polyp of the anus
fibromuscular dysplasia
fibrous dysplasia
filariasis
fluoride poisoning
FLVCR1-related retinopathy with or without ataxia
follicular mucinosis
Fontaine progeroid syndrome
forebrain
fox fordyce disease
FRAXE intellectual disability
free sialic acid storage disease
Freeman-Sheldon syndrome
Friedreich ataxia
frontal lobe
Fuchs endothelial corneal dystrophy
Fuchs' endothelial dystrophy
fumaric aciduria
fungal esophagitis
gamma-delta intraepithelial T cell
ganglion
gas gangrene
gastrocnemius
gastroenteritis
gastrointestinal defects and immunodeficiency syndrome 1
gastrointestinal stromal tumor
gastrointestinal tuberculosis
gastrula stage
GATA2 deficiency with susceptibility to MDS/AML
Generalized arterial tortuosity
generalized resistance to thyroid hormone
genital herpes
geography-based population category
giant cell reparative granuloma
glabellar hemangioma
glial cell
glioblastoma multiforme
global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome
glossopharyngeal neuralgia
glucosephosphate dehydrogenase deficiency
glycine N-methyltransferase deficiency
glycogen storage disease due to acid maltase deficiency, infantile onset
glycoprotein biosynthetic process
glycoprotein metabolic process
glyphosate
GM2
gnathomiasis
GNPTG-mucolipidosis
goblet cell
gonosome anomaly
Gorham-Stout disease
Granulocytic Sarcoma
granuloma annulare
granulosa cell
granulosa cell tumor
Graves disease
Gray matter heterotopia
gremlin-1
gremlin-1 (human)
Griscelli syndrome type 2
growth hormone-secreting pituitary adenoma
GTP cyclohydrolase I deficiency
Gyrate atrophy of choroid and retina
Haemophilus influenzae meningitis
Hailey-Hailey disease
Hamartoma
Harlequin ichthyosis
head
head mesenchyme
Heat Stroke
HELLP syndrome
hemangioblastoma
Hematochezia
hemochromatosis type 2
hemoglobin A1 measurement
hemophagocytic syndrome
hemophilia A
Hennekam-Beemer syndrome
Henoch-Schoenlein purpura
hepatic tuberculosis
Hepatoblastoma
hepatocellular adenoma
hepatocellular carcinoma
hereditary amyloidosis
hereditary ataxia
hereditary episodic ataxia
hereditary hemochromatosis type 1
hereditary motor and sensory neuropathy, Okinawa type
hereditary nephritis
hereditary site-specific ovarian cancer syndrome
hereditary spastic paraplegia 4
hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1
Hibiscus chlorotic ringspot virus infection
hidradenitis suppurativa
High anterior hairline
high-grade astrocytoma with piloid features
hindbrain
hippocampal CA3 volume
Hirschmanniella oryzae
histiocytoma, Angiomatoid fibrous
holoprosencephaly-craniosynostosis syndrome
Holt-Oram syndrome
Hot flashes
HSD10 disease, neonatal type
human prion disease
humero-radio-ulnar synostosis
Hurler syndrome
Hydrocephalus with stenosis of the aqueduct of Sylvius
hymenolepiasis
hyomandibula
hypercementosis
hyperekplexia 4
Hyperpituitarism
hyperplastic polyposis syndrome
hypocretin deficiency
hypoplastic right heart syndrome
hypothalamus
iatrogenic botulism
ichthyosis
ichthyosis vulgaris
idiopathic CD4 lymphocytopenia
idiopathic osteonecrosis of the femoral head
ileocolitis
ilium
immune-mediated adverse reaction
immunodeficiency 32B
immunodeficiency 82 with systemic inflammation
immunodeficiency 98 with autoinflammation, X-linked
inclusion body myositis
infectious myxomatosis
infectious otitis interna
infectious otitis media
inflorescence
inherited glutathione synthetase deficiency
inherited ichthyosis
initiator methionine
insulin
intellectual developmental disorder with cardiac defects and dysmorphic facies
intellectual developmental disorder with dysmorphic facies and ptosis
intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies
intellectual developmental disorder with gastrointestinal difficulties and high pain threshold
intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies
intellectual disability with language impairment
intellectual disability-severe speech delay-mild dysmorphism syndrome
intercellular adhesion molecule 1/3
Interictal EEG abnormality
intermediate monocyte
interneuron
interstitial emphysema
Intervertebral Disc Displacement
intestinal bulb
intracranial berry aneurysm
intracranial embolism
intraepithelial lymphocyte
Invasive Breast Carcinoma
invasive breast ductal carcinoma
invertebrate limb
iris melanoma
ischemia reperfusion injury
ischemic cardiomyopathy
Isolated polycystic liver disease
Ito hypomelanosis
ivermectin
Joubert syndrome with ocular defect
juvenile idiopathic arthritis
Juvenile Myelomonocytic Leukemia
juvenile myoclonic epilepsy
juvenile polyposis of infancy
juvenile type testicular granulosa cell tumor
Juvenile Xanthogranuloma
juxtacortical osteosarcoma
Kaposi's sarcoma
KCNH1 associated disorder
Kidney Medullary Carcinoma
kidney Wilms tumor
Klinefelter's syndrome
knee joint
kuru
lactose
larval protruding mouth
laryngeal squamous cell carcinoma
larynx liposarcoma
late-onset Alzheimers disease
Leiomyoma, Epithelioid
leiomyosarcoma of the cervix uteri
Lesch-Nyhan syndrome
lethal recessive chondrodysplasia
leukoplakia of gingiva
leukoplakia of tongue
Leydig cell
lichen planopilaris
linear and whorled nevoid hypermelanosis
linear atrophoderma of Moulin
linear nevus sebaceous syndrome
lip and oral cavity carcinoma
lipoic acid synthetase deficiency
lipoma of colon
liver cavernous hemangioma
liver lymphoma
lobe attachment
long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
longissimus thoracis muscle
loose anagen syndrome
Low anterior hairline
low-density lipoprotein
lung meningioma
lymphoid tissue
lysosome
Machado-Joseph disease
major salivary gland
Major Salivary Gland Mucoepidermoid Carcinoma
malaria
malathion
malignant choroid melanoma
malignant hyperthermia, susceptibility to, 1
malignant peripheral nerve sheath tumor
malignant phyllodes tumor
malignant testicular germ cell tumor
MALT lymphoma
Marchiafava-Bignami Disease
Marfan syndrome
marginal zone B-cell lymphoma
mast cell
Mast Cell Neoplasm
mast-cell leukemia
mastocytoma
Maternal diabetes
maternal uniparental disomy of chromosome 1
maternal uniparental disomy of chromosome 13
maternal uniparental disomy of chromosome 2
maternal uniparental disomy of chromosome 20
maternal uniparental disomy of chromosome 4
maternal uniparental disomy of chromosome 9
mature gamma-delta T cell
mature T-cell and NK-cell non-Hodgkin lymphoma
Mazabraud syndrome
McCune-Albright syndrome
MED12-related intellectual disability syndrome
mediastinal neural neoplasm
mediastinal schwannoma
medulloblastoma with extensive nodularity
megakaryocyte-erythroid progenitor cell
megalencephaly-capillary malformation-polymicrogyria syndrome
megalocornea-intellectual disability syndrome
megasexuality
melanoma
Meloidogyne graminicola
melorheostosis
Meniere disease
meningioma
meralgia paresthetica
Merkel cell skin cancer
mesial temporal lobe epilepsy with hippocampal sclerosis
mesoblastic nephroma
mesodermal cell
metaphyseal anadysplasia
metastatic carcinoma in the bone
methylcobalamin deficiency type cblG
Middle East respiratory syndrome
mild hypophosphatasia
Mirror image polydactyly
mitotic cell cycle
mixed connective tissue disease
molybdenum cofactor sulfurase
molybdenum cofactor sulfurase (human)
Mono Mac 6
monogenic diabetes
morphine
Morvan syndrome
mosaic
mosaic genome-wide paternal uniparental disomy
mosaic loss of chromosome X measurement
mosaic loss of chromosome Y measurement
mosaic monosomy X
mosaic SMO syndrome
mosaic trisomy 1
mosaic trisomy 10
mosaic trisomy 12
mosaic trisomy 13
mosaic trisomy 14
mosaic trisomy 15
mosaic trisomy 16
mosaic trisomy 17
mosaic trisomy 18
mosaic trisomy 2
mosaic trisomy 20
mosaic trisomy 21
mosaic trisomy 22
mosaic trisomy 3
mosaic trisomy 4
mosaic trisomy 5
mosaic trisomy 6
mosaic trisomy 7
mosaic trisomy 8
mosaic trisomy 9
mosaic variegated aneuploidy syndrome
mosaic variegated aneuploidy syndrome 1
mosaic variegated aneuploidy syndrome 2
mosaic variegated aneuploidy syndrome 3
mosaic variegated aneuploidy syndrome 4
mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition
mosaic vs complete
Mosaic-Seq
MOSPD1 (human)
mosquito bite measurement
mosquito bite reaction itch intensity measurement
mosquito bite reaction size measurement
mosquito-borne hemorragic fever
mosquito-borne viral encephalitis
Mossi
motile sperm domain-containing protein 1
motile sperm domain-containing protein 1 (human)
mouth mucous membrane leukoplakia
Moyamoya disease with early-onset achalasia
mucocutaneous Leishmaniasis
mucocutaneous lymph node syndrome
mucolipidosis type III, alpha/beta
mucopolysaccharidosis type 1
mucopolysaccharidosis type 2, severe form
mucosa
mucosulfatidosis
Muir-Torre syndrome
multidrug-resistant tuberculosis
multifocal choroiditis
multiple congenital anomalies due to 14q32.2 maternally expressed gene defect
multiple endocrine neoplasia type 1
multiple symmetric lipomatosis
muscularis mucosa
mycosis fungoides
mycosis fungoides and variants
myeloblast
myelocyte
myelomeningocele
Myelopathy
myiasis
myocarditis
myoclonus, familial
myosclerosis
myxoid/round cell liposarcoma
nasal cavity and paranasal sinus squamous cell carcinoma
necrotizing enterocolitis
Nematoda
neocortex
neonatal intrahepatic cholestasis due to citrin deficiency
neoplasm of mature B-cells
neovascular glaucoma
nephrolithiasis
nephropathic infantile cystinosis
neuroaspergillosis
neuroblastoma
neurodevelopmental disorder with hypotonia, brain anomalies, distinctive facies, and absent language
neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities
neurodevelopmental disorder with or without anomalies of the brain, eye, or heart
neurofibrosarcoma
Neuropathic spinal arthropathy
neuropathy, hereditary motor and sensory, type vib
neutral lipid storage disease
neutrophil
nevus
Nevus of Ito
Nevus sebaceous
nevus, epidermal
Newcastle disease
Niemann-Pick disease, type C2
nodular nonsuppurative panniculitis
noise-induced hearing loss
non-alcoholic steatohepatitis
Non-Cutaneous Melanoma
Non-hereditary late-onset primary lymphedema
non-melanoma skin carcinoma
norfloxacin
notochord
nucleus
NUT midline carcinoma
obesity due to CEP19 deficiency
ochratoxin A
Ocular Sebaceous Carcinoma
ocular toxoplasmosis
oculocutaneous albinism
oculocutaneous albinism type 1A
oculocutaneous albinism type 2
oligoarticular juvenile idiopathic arthritis
oligoasthenoteratozoospermia
olivopontocerebellar atrophy-deafness syndrome
OPA1-related optic atrophy with or without extraocular features
optic nerve glioblastoma
optic tract astrocytoma
oral cavity carcinoma
oral squamous cell carcinoma
Orofacial cleft
Ossifying Fibromyxoid Tumor
osteoarthritis, spine
osteopathia striata-pigmentary dermopathy-white forelock syndrome
osteosarcoma
otitis externa
Otitis media
otopalatodigital syndrome spectrum disorder
outer membrane
ovarian adenocarcinoma
ovarian cancer
ovarian carcinoma
Ovarian Dysgerminoma
ovarian granulosa cell tumor
ovarian granulosa tumour
Ovarian Leydig Cell Tumor
ovarian malignant mesothelioma
ovarian mixed germ cell neoplasm
Ovarian Yolk Sac Tumor
overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes
palsy
Pancoast tumor
pancreatic acinar cell
pancreatic ductal cell
pancreatic epsilon cell
pancreatic intraductal papillary-mucinous neoplasm
pancreatic neoplasm
paneth cell
pantothenate kinase-associated neurodegeneration
papillary hidradenoma
papillary renal cell carcinoma
papillary squamous carcinoma
papillary thyroid carcinoma
Parachordoma
paracoccidioidomycosis
paraneoplastic polyneuropathy
paraplegia-intellectual disability-hyperkeratosis syndrome
parasitic ectoparasitic infectious disease
parasympathetic nervous system
Parkinson disease
Parotid Gland Pleomorphic Adenoma
parp inhibitor response
partial deletion of the long arm of chromosome 2
partial deletion of the long arm of chromosome 4
partial deletion of the long arm of chromosome 6
partial deletion of the long arm of chromosome 7
partial deletion of the long arm of chromosome 8
partial deletion of the short arm of chromosome 1
partial deletion of the short arm of chromosome 7
partial deletion of the short arm of chromosome 8
partial duplication of the long arm of chromosome 12
partial duplication of the long arm of chromosome 15
partial duplication of the long arm of chromosome 2
partial duplication of the long arm of chromosome 4
partial duplication of the long arm of chromosome 6
partial duplication of the long arm of chromosome 7
partial duplication of the long arm of chromosome X
partial duplication of the short arm of chromosome 16
partial duplication of the short arm of chromosome 2
partial duplication of the short arm of chromosome 7
partial duplication of the short arm of chromosome 8
patellofemoral pain syndrome
Patent ductus arteriosus - bicuspid aortic valve - hand anomalies
patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome
paternal uniparental disomy of chromosome 1
paternal uniparental disomy of chromosome 13
paternal uniparental disomy of chromosome 20
paternal uniparental disomy of chromosome 21
paternal uniparental disomy of chromosome 5
paternal uniparental disomy of chromosome 7
peak expiratory flow
Pectobacterium carotovorum infection
Pelizaeus-Merzbacher disease, connatal form
Pelvic Inflammatory Disease
pemphigoid gestationis
pemphigus foliaceus
pemphigus vulgaris
perceived unattractiveness to mosquitos measurement
peripartum cardiomyopathy
peritonitis
Periventricular heterotopia
peroxisome
Pfeiffer syndrome type 1
phagocyte
pharyngitis
phenylketonuria
pheochromocytoma-paraganglioma
Phlebotomus fever
Phonic tics
phosphatidylglycerophosphatase and protein-tyrosine phosphatase 1 (human)
phyllid
pilocytic astrocytoma
Pilomatrixoma
Pineoblastoma
pituitary apoplexy
pityriasis rosea
pleural neoplasm
PMM2-congenital disorder of glycosylation
pneumococcal meningitis
pneumocystosis
pneumonia caused by pseudomonas aeruginosa infection
Poland syndrome
polyarteritis nodosa
polyarteritis nodosa, childhoood-onset
polydactyly of a biphalangeal thumb
pontocerebellar hypoplasia type 2
Popliteal synovial cyst
porphyria
porphyria cutanea tarda
portal hypertension
Postaxial foot polydactyly
posterior lateral line system
posterior meningocele
posterior urethral valve
posterior uveitis
postprandial hypotension
postweaning multisystemic wasting syndrome
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel protein
preaxial polydactyly of fingers
precursor B-cell acute lymphoblastic leukemia
prefrontal cortex
pregnancy associated osteoporosis
premature chromatid separation trait
presomitic mesoderm
presumptive hindbrain
primary bone lymphoma
Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type
primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency
primary intraosseous venous malformation
primary localized amyloidosis
primary lymphoma of the conjunctiva
primary metabolic process
primary peritoneal carcinoma
Prime editing
progressive external ophthalmoplegia
progressive multifocal leukoencephalopathy
Prolactin-Producing Pituitary Gland Adenoma
prostaglandin E2
prostatic acinar adenocarcinoma
protein array
protein-tyrosine phosphatase mitochondrial 1
prothoracic gland
proximal convoluted tubule
prurigo nodularis
Psoas abscess
psoriasis vulgaris
psoriatic arthritis, susceptibility to, 1
Pulmonary arterial hypertension associated with congenital heart disease
Pulmonary arteriovenous malformation
Pulmonary bulla
pulmonary fibrosis and/or bone marrow failure, telomere-related, 1
pulmonary fibrosis, and/or bone marrow failure, telomere-related, 5
Pulmonary Infarction
pulmonary sulcus neoplasm
pulmonary tuberculosis
pulse wave reflection index measurement
Purpura Fulminans
putamen
pyelonephritis
pyoderma gangrenosum
pyruvate dehydrogenase E1-alpha deficiency
Quechua
quercetin
Radial ray deficiency
rasopathy
recessive dystrophic epidermolysis bullosa
reflex epilepsy
reflex sympathetic dystrophy
region
relapsing-remitting multiple sclerosis
renal colic
renal hypodysplasia/aplasia 3
Respiratory Syncytial Virus Infection
response to endocrine therapy
reticular dysgenesis
retinal capillary malformation
retinal macular dystrophy type 2
retinoblastoma
rhabdomyosarcoma with mixed embryonal and alveolar features
rheumatic fever
rheumatic fever nodule
rheumatic heart disease
rhodopsin-like G-protein coupled receptor
Rickets
ring chromosome 1
ring chromosome 18
ring chromosome 20
ring chromosome 21
ring chromosome 22
ring chromosome 4
ring chromosome 9
ring chromosome Y
rolandic epilepsy-speech dyspraxia syndrome
Roseolovirus infectious disease
rosette-forming glioneuronal tumor of fourth ventricule
rotator cuff tear
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
ryr1-related disorders
salivary gland mucoepidermoid carcinoma
Salivary Gland Pleomorphic Adenoma
salpingitis
SAPHO syndrome
SATB2 associated disorder
Schwann cell
selective IgA deficiency disease
self-limited epilepsy with autonomic seizures
septicemic plague
serous cystadenofibroma
serum albumin
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency
sex chromosome disorder of sex development
shoot apex
short chain acyl-CoA dehydrogenase deficiency
Short chin
Short distal phalanx of finger
Short distal phalanx of toe
shoulder impingement syndrome
sialadenitis
sialolithiasis
sialuria
Sifrim-Hitz-Weiss syndrome
silicosis
sirenomelia
skin basal cell carcinoma
skin mastocytoma
skin squamous cell carcinoma
SLC35A2-congenital disorder of glycosylation
small cell carcinoma
Small Intestinal Enteropathy-Associated T-Cell Lymphoma
smooth muscle
Soft Tissue Neoplasm
solitary fibrous tumor
southeast Asian ovalocytosis
spastic diplegia
spastic paraplegia-severe developmental delay-epilepsy syndrome
spermatocytic seminoma
spinal cord neoplasm
spinal meningioma
Spinocerebellar ataxia type 3
spinocerebellar ataxia type 6
spinocerebellar ataxia with epilepsy
spitz nevus
spondyloarthropathy
spondyloepimetaphyseal dysplasia, Handigodu type
spondylometaphyseal dysplasia, 'corner fracture' type
sporadic Creutzfeld Jacob disease
squamous epithelium
squamous papilloma
St. Louis encephalitis
stage I endometrioid carcinoma
stage II endometrioid carcinoma
strand of hair
streptococcal pneumonia
Striae distensae
strongyloidiasis
Sturge-Weber syndrome
SU-DHL-2
subcorneal pustular dermatosis
subependymal giant cell astrocytoma
substantia nigra
succinic semialdehyde dehydrogenase deficiency
suicidal ideation
superficial fascia
supranuclear palsy, progressive, 1
susceptibility to malaria
susceptibility to partial acquired lipodystrophy
Swan neck-like deformities of the fingers
swine influenza
sympathetic nervous system
synovial bursa
Synovial Chondromatosis
synovial sarcoma
systemic lupus erythematosus
systemic scleroderma
T-cell surface glycoprotein CD8 alpha chain
T-cell surface glycoprotein CD8 beta chain
T-lymphoblastic lymphoma
taurodontism
temporal lobe epilepsy
Teratoma with Malignant Transformation
terminal ileum
Testicular Embryonal Carcinoma
Testicular torsion
Testicular Yolk Sac Tumor
Tetraamelia - multiple malformations
tetraamelia-multiple malformations syndrome
tetradecanoic acid
tetrasomy 12p
tetrasomy 5p
tetrasomy 9p
thrombophilia due to activated protein C resistance
thrombotic thrombocytopenic purpura
Thymoma
tibial neuropathy
tissue-resident macrophage
tongue squamous cell carcinoma
Toxic Nodular Goiter
toxoplasmosis
trabecula
tracheobronchial amyloidosis
transient neonatal diabetes mellitus
transient neonatal diabetes, dominant/recessive
trichoblastoma
tricuspid valve prolapse
triploidy
trisomy 20p
trisomy 22
trisomy 8q
tropical sprue
tuberculosis
tuberculous peritonitis
tubular aggregate myopathy
tubulinopathy
tubulovillous adenoma
tufted angioma
Tularemia
Tumor Lysis Syndrome
tumor predisposition syndrome 2
typhus
Undifferentiated Gallbladder Carcinoma
undifferentiated high grade pleomorphic sarcoma of bone
Undifferentiated Ovarian Carcinoma
uremia
ureterolithiasis
urinary tract infection
urothelial cell
uterine corpus choriocarcinoma
uterine sarcoma
Uveal Melanoma
Vaginal Squamous Cell Carcinoma
variant Creutzfeldt-Jakob disease
vasculitis, lymphocytic, nodular
Vasovagal syncope
Venezuelan equine encephalitis
ventral striatum
verrucous carcinoma
vertebrate G-type lysozyme
villous adenoma
viral encephalitis
viral respiratory tract infection
vitamin B12 measurement
vitamin E metabolic process
volumetric bone mineral density
von Willebrand disease 3
vulvar neuroendocrine carcinoma
Warthin Tumor
Waterhouse-Friderichsen syndrome
West Nile encephalitis
West Nile fever
Western equine encephalitis
Wiedemann-Steiner syndrome
Williams syndrome
Wolff-Parkinson-White Syndrome
Wolman disease
X-linked chondrodysplasia punctata 2
X-linked dominant chondrodysplasia punctata
X-linked hydrocephalus with stenosis of the aqueduct of Sylvius
X-linked intellectual disability-corpus callosum agenesis-spastic quadriparesis syndrome
xanthogranulomatous pyelonephritis
Xeroderma pigmentosum complementation group C
XY type gonadal dysgenesis-associated anomalies syndrome
xylose
Yellow Nail Syndrome
Young adult-onset Parkinsonism
young-onset Parkinson disease
zeaxanthin measurement
Zellweger spectrum disorders
Zellweger syndrome
Zika virus infectious disease
GO: Biological Process
1,2-diacyl-sn-glycero-3-phosphocholine metabolic process
2-oxoglutarate decarboxylation to succinyl-CoA
analia development
analia morphogenesis
anterior lateral line development
anterior lateral line system development
anthocyanin-containing compound metabolic process
appendage segmentation
astrocyte cell migration
astrocyte development
astrocyte differentiation
avascular cornea development in camera-type eye
basidiospore formation
bud dormancy process
cell wall assembly
cell wall biogenesis
cell wall macromolecule metabolic process
cell wall organization
cellular response to norepinephrine stimulus
cellular response to redox state
cerebellar granular layer development
cerebellar granular layer formation
cerebellar granular layer maturation
cerebellar granular layer morphogenesis
cerebellar granular layer structural organization
collenchyma cell differentiation
cotranslational protein targeting to membrane
creatine biosynthetic process
cytoplasm to vacuole targeting by the Cvt pathway
detection of redox state
dormancy process
dorsal closure, elongation of leading edge cells
dorsal closure, leading edge cell differentiation
dorsal closure, leading edge cell fate commitment
dosage compensation by hyperactivation of X chromosome
dosage compensation by inactivation of X chromosome
embryonic hemocyte differentiation
embryonic pelvic fin morphogenesis
entry into dormancy
epigenetic programing of male pronucleus
ergosterol metabolic process
establishment of blood-brain barrier
establishment of endothelial blood-brain barrier
establishment of glial blood-brain barrier
estrous cycle
exit from dormancy
exocytosis
eye photoreceptor cell differentiation
female analia development
female analia morphogenesis
flavonol biosynthetic process
flavonol metabolic process
forebrain astrocyte development
forebrain astrocyte differentiation
gamma-1,2,3,4,5,6-hexachlorocyclohexane metabolic process
gap junction assembly
gastrulation
germ tube formation
germarium-derived female germ-line cyst formation
glucosinolate metabolic process
glutamate secretion
glycoprotein biosynthetic process
glycoprotein catabolic process
glycoprotein metabolic process
head development
head morphogenesis
hemocyte development
hemocyte differentiation
hemocyte migration
hemocyte proliferation
inactivation of paternal X chromosome by genomic imprinting
Kupffer's vesicle development
lamina terminalis formation
larval lymph gland hemocyte differentiation
lateral line development
lateral line system development
lens epithelial cell proliferation
lens fiber cell differentiation
long-day photoperiodism
long-day photoperiodism, flowering
lysosome organization
maintenance of dormancy
male analia development
male analia morphogenesis
mechanosensory lateral line system development
metanephric proximal convoluted tubule development
microtubule-dependent intracellular transport of viral material
microtubule-dependent intracellular transport of viral material towards cell periphery
mitotic cell cycle
negative regulation of glycoprotein biosynthetic process
negative regulation of hemocyte proliferation
negative regulation of neutrophil chemotaxis
negative regulation of pyruvate decarboxylation to acetyl-CoA
negative regulation of sporangium development
nematode male tail tip morphogenesis
neutrophil chemotaxis
norepinephrine secretion
notochord development
notochord morphogenesis
parasympathetic nervous system development
pelvic fin morphogenesis
photosystem II assembly
plant parenchymal cell differentiation
pollen development
polymyxin transport
positive regulation of glycoprotein biosynthetic process
positive regulation of hemocyte proliferation
positive regulation of neutrophil chemotaxis
positive regulation of odontogenesis of dentin-containing tooth
positive regulation of pyruvate decarboxylation to acetyl-CoA
positive regulation of sporangium development
post-embryonic pelvic fin morphogenesis
posterior lateral line development
posterior lateral line system development
postganglionic parasympathetic fiber development
postsynaptic density protein 95 clustering
primary metabolic process
primary spermatocyte growth
protein processing in phagocytic vesicle
proximal convoluted tubule development
pyruvate decarboxylation to acetyl-CoA
random inactivation of X chromosome
receptor-mediated endocytosis
reductive tricarboxylic acid cycle
regulation of cell wall macromolecule metabolic process
regulation of gastrulation
regulation of glycoprotein biosynthetic process
regulation of hemocyte proliferation
regulation of neutrophil chemotaxis
regulation of odontogenesis of dentin-containing tooth
regulation of primary metabolic process
regulation of pyruvate decarboxylation to acetyl-CoA
regulation of sporangium development
reproductive blastospore formation
response to norepinephrine
response to redox state
response to stilbenoid
retinal metabolic process
seed dormancy process
short-day photoperiodism
short-day photoperiodism, flowering
skeletal muscle contraction
skin development
skin morphogenesis
sno(s)RNA metabolic process
sphingosine biosynthetic process
sphingosine catabolic process
sphingosine metabolic process
spicule insertion
starch biosynthetic process
starch catabolic process
starch metabolic process
stomach pylorus smooth muscle contraction
sympathetic nervous system development
synergid death
T-helper 1 type immune response
T-helper 17 type immune response
temperature compensation of the circadian clock
tetrahydrofuran catabolic process
tongue development
tongue morphogenesis
tRNA aminoacylation
tRNA aminoacylation for mitochondrial protein translation
tRNA aminoacylation for nonribosomal peptide biosynthetic process
tRNA aminoacylation for protein translation
type 2 immune response
uredospore formation
vacuolar protein processing
vitamin E biosynthetic process
vitamin E metabolic process
xyloglucan biosynthetic process
xyloglucan metabolic process
zearalenone biosynthetic process
GO: Cellular Component
90S preribosome
actin filament
alphav-beta3 integrin-collagen alpha3(VI) complex
amyloid-beta complex
anaphase-promoting complex
asymmetric synapse
axolemma
axonemal central apparatus
axonemal central bridge
axonemal central pair
axonemal central pair projection
bacterial-type flagellum basal body, distal rod
basal layer of collagen and cuticulin-based cuticle extracellular matrix
basal ring of apical complex
bounding membrane of organelle
box H/ACA RNP complex
box H/ACA telomerase RNP complex
cell wall
cellular bud neck septin collar
cellularization cleavage furrow invagination front
central vacuole
centrosome
cerebellar mossy fiber
chaperonin ATPase complex
collagen type I trimer
core mediator complex
cytoophidium
dendrite
dentate gyrus mossy fiber
dinoflagellate antapex
dinoflagellate apex
DNA topoisomerase IV complex
ferritin complex
fibrillar center
GDP-mannose pyrophosphorylase complex
germ tube
growth cone
helical viral capsid
hippocampal mossy fiber
hippocampal mossy fiber expansion
hippocampal mossy fiber to CA3 synapse
histone mRNA stem-loop binding complex
host cell centrosome
host cell late endosome
host cell lysosome
host cell peroxisome
host cell wall
host outer membrane
HSP90-CDC37 chaperone complex
interstitial hexagonal collagen network
keratin filament
large latent transforming growth factor-beta complex
late endosome
low-density lipoprotein receptor complex
lysosome
mediator complex
MHC class Ib protein complex
MHC protein complex
mossy fiber rosette
MsbA transporter complex
nematosome
new cell pole
nucleus
old cell pole
organelle inner membrane
osmiophilic body
outer kinetochore
outer membrane
pectic matrix
peri-centrosomal recycling endosome
peroxisome
polar ring of apical complex
procollagen-proline 4-dioxygenase complex
Prp19 complex
radial spoke 1
radial spoke 3
rhabdomere
RNA polymerase I complex
RNA polymerase II, core complex
RNA polymerase III complex
RNA polymerase V complex
RNAi effector complex
secondary cell wall
slime layer
small-subunit processome
specific granule
specific granule lumen
specific granule membrane
sperm cytoplasmic droplet
subapical complex
succinate-CoA ligase complex (ADP-forming)
super elongation complex
transcription factor TFIID complex
type III protein secretion system complex
U1 snRNP
U11 snRNP
U12 snRNP
U2 snRNP
U4 snRNP
U4atac snRNP
U5 snRNP
U6 snRNP
U6atac snRNP
unicellular trichome apex
unicellular trichome tip
viral capsid, major subunit
GO: Molecular Function
11-cis retinal binding
all-trans retinal binding
CAAX-protein geranylgeranyltransferase activity
CD70 receptor binding
CRD domain binding
diazepam binding
growth factor activity
histone H1 reader activity
histone H2A reader activity
histone H2B reader activity
histone H3 reader activity
histone H4 reader activity
lactoferrin receptor activity
MAP kinase activity
polymyxin transmembrane transporter activity
retinal binding
RNA polymerase I general transcription initiation factor activity
RNA polymerase II general transcription initiation factor activity
telomeric repeat-containing RNA binding
tubulin N-acetyltransferase activity
vitamin E binding
HP: Human Phenotype
Abdominal colic
Abnormal adiponectin level
Abnormal cartilage collagen
Abnormal CD69 upregulation upon TCR activation
Abnormal circulating eicosanoid concentration
Abnormal circulating globulin concentration
Abnormal four chamber view of the fetal heart
Abnormal hamate bone morphology
Abnormal hypopharynx morphology
Abnormal nasal base norphology
Abnormal occipitofrontal diameter
Abnormal platelet granule secretion
Abnormal platelet volume
Abnormal retinol-binding protein level
Abnormal ventricular axis
Abnormality of secondary sexual hair
Abnormality of the premaxilla
Absent Birbeck granules in Langerhans cells
Absent posterior alpha rhythm
Accessory spleen
Agammaglobulinemia
Allantoic cyst
Altered location of the longitudinal column in the fibrous sheath
Ameliorated by ethosuximide
Anencephaly
Angiokeratoma circumscriptum naeviforme
Anti-bactericidal/permeability-increasing protein antibody positivity
Anti-CV2/CRMP5 antibody positivity
Aplasia cutis congenita
Atrichia
Atrophy/Degeneration affecting the cerebrum
Autonomic epileptic aura
Balanced double aortic arch
Bifid uvula
Bilateral basilar pulmonary fibrosis
Bladder rupture
Blepharochalasis
Blood group
Broncholith
Budd-Chiari syndrome
Bunionette deformity
Candida esophagitis
Cardiac teratoma
Central nervous system axonal spheroid
Cerebral cortical microinfarct
Cerebriform connective tissue nevus
Cervical intraepithelial neoplasia
Choanal atresia
Choroid plexus carcinoma
Chronic (near) absent circulating IgG1
Chronic (near) absent circulating IgG2
Chronic (near) absent circulating IgG3
Chronic (near) absent circulating IgG4
Chronic absent circulating IgD
Chronic absent circulating IgE
Chronic absent circulating total IgG
Civatte bodies
Cleft maxillary alveolar ridge
Colonization of follicles by lymphoma cells
Conjunctival icterus
Cortical myoclonus
Cortical superficial CNS hemosiderin deposition
Decreased adiponectin level
Deep venous thrombosis
Delayed ability to sit
Delayed ability to stand
Delayed ability to walk
Dermal sinus tract
Dextrotransposition of the great arteries
Disseminated candidiasis
Diverticulosis of trachea
Dysembryoplastic neuroepithelial tumor
Eccrine syringofibroadenoma
Ectopic ureteral orifice
Elevated circulating lysosphingomyelin concentration
Elevated circulating porphyrin concentration
Elevated umbilical artery pulsatility
Enlarged tectum
Enterocolitis
Epithelioid hemangioma
Erythroderma
Expiratory air trapping
Extrapulmonary tuberculosis
Extremities cold to touch
Febrile seizure (within the age range of 3 months to 6 years)
Febrile seizure outside the age of 3 months to 6 years
Fetal abdominal cyst
Fetal pleural effusion
Follicular conjunctivitis
Food allergy
Fordyce angiokeratoma
Gastrointestinal desmoid tumor
Generalized arterial tortuosity
Generalized dystonia
Glomerular basement membrane amyloid spicule
Glomerular endothelial tubuloreticular inclusion
Gray matter heterotopia
Hamartoma
Hematochezia
High anterior hairline
History of congenital CMV infection
History of recent central venous catheter
History of thumb sucking past the age of four years
Hopelessness
Hot flashes
Hot water-induced seizure
Hyperpituitarism
Ichthyosis follicularis
Immediate-type hypersensitivity drug reaction
Impaired executive functioning
Inclusion body fibromatosis
Increased adiponectin level
Increased anti-insect IgE antibody level
Increased extraneuronal autofluorescent lipopigment
Increased neuronal autofluorescent lipopigment
Increased QRS voltage
Infratentorial superficial CNS hemosiderin deposition
Interictal EEG abnormality
Interstitial emphysema
Intra-epidermal blistering
Intraepidermal microabscess formation
Juvenile aseptic necrosis
Juvenile type ovarian granulosa cell tumor
Juxtaphrenic peak
Keratoacanthoma
Lacrimal duct atresia
Lipomyelomeningocele
Lobar holoprosencephaly
Low anterior hairline
Lunotriquetral ligament tear
Lupus nephritis
Lymph-node follicular lysis
Lymph-node lymphocyte monocytoid morphology
Lymphoid nodular hyperplasia
Macrodactyly
Macular dots
Macular edema
Malignant mesothelioma
Maternal diabetes
Maternal retinal mottling
Maturity-onset diabetes of the young
Merkel cell skin cancer
Mesangial Immune complex deposition
Mesangial microfibril deposition
Metaphyseal chevron deformity
Metatarsal head osteochondrosis
Meteorism
Mirror image polydactyly
Mosaic attenuation pattern in lung
Mosaic attenuation pattern on pulmonary HRCT
Mosaic central corneal dystrophy
Mosaic corneal dystrophy
Mosaic pulmonary attenuation pattern
Myelopathy
Myocardial bridging
Neural tube defect
Neuroblastoma
Neurocytoma
Neuroepithelial cyst
Neuropathic spinal arthropathy
Nevus flammeus nuchae
Nevus sebaceous
Nonspecific interstitial pneumonia
Nummular eczema
Oligodendroglioma
Opisthotonus
Oral melanoacanthoma
Orofacial cleft
Os trigonum
Osteoma
Ovarian cystadenoma
Overfriendliness
Peripheral axon spheroid formation
Peritoneal mesothelioma
Periventricular heterotopia
Periventricular leukomalacia
Persistent human papillomavirus infection
Phonic tics
Phosphaturic mesenchymal tumor
Pilocytic astrocytoma
Pleomorphic xanthoastrocytoma
Pleural mesothelioma
Pleuropulmonary blastoma
Polyminimyoclonus
Popliteal synovial cyst
Porcelain gallbladder
Positive heel squeeze test
Positive skin fungus test
Postaxial foot polydactyly
Posterior capsule opacification
Preauricular cyst
Pressure ulcer
Presyncope
Primum atrial septal defect
Progressive massive fibrosis
Pulmonary arteriovenous malformation
Pulmonary bulla
Pulmonary oligemia
Pulmonary parenchymal band
Pulmonary pneumatocele
Radial ray deficiency
Recurrent corneal erosions
Recurrent gingivitis
Recurrent meningococcal disease
Recurrent Neisserial infections
Recurrent, involuntary, and intrusive distressing memories
Renal interstitial amyloid deposits
Requires heterozygosity
Restless legs
Retinal dots
Rhabdoid tumor
Rheumatoid nodule
Rickets
Rounded atelectasis
Salter II fracture
Scapholunate ligament tear
Schizophrenia
Short chin
Short distal phalanx of finger
Short distal phalanx of toe
Single second heart sound
Skeletal muscle hyperechogenicity
Skin nodule
Soft tissue neoplasm
Spontaneous lens capsule rupture
Startle-induced seizure
Striae distensae
Superficial blush-like subcutaneous fatty lesions
Swan neck-like deformities of the fingers
Synovial sarcoma
Tall chin
Tarlov cyst
Tertiary hyperparathyroidism
Testicular torsion
Thin-cap fibroatheroma
Third ventricle colloid cyst
Thymic cyst
Transitional-cell carcinoma of the ureter
Triangular epiphysis
Triggered by poison ivy, poson oak, or sumac
True hermaphroditism
Type III radial ray deficiency
Type IV radial ray deficiency
Typified by somatic mosaicism
Urinoma
Vascular granular osmiophilic material deposition
Vasovagal syncope
Ventricular septal defect
Verrucae
Verrucous epidermal nevus
Widely spaced teeth
Yellow nodule
MI: Molecular Interactions
cisphenotypic co-suppressing genetic interaction
cisphenotypic genetic suppression
cisphenotypic genetic suppression (complete)
cisphenotypic genetic suppression (partial)
cisphenotypic inter-suppressing genetic interaction
complex recommended name
converging genetic epistasis
cosedimentation through density gradient
cyp-450 inhibition
diffusion coefficient
dimethylsulphate footprinting
dna methyltransferase tag
dna overhang
far western blotting
filamentous phage display
fluorescein-5-maleimide label
full identification by DNA sequencing
genetic suppression (partial)
genetic suppression (sensu unexpected)
light scattering
long non-coding ribonucleic acid
maximal genetic epistasis
minimal genetic epistasis
mrna display
mutual genetic enhancement
mutual genetic enhancement (sensu unexpected)
mutual genetic over-suppression
mutual genetic suppression (complete)
pir
protein cross-linking with a bifunctional reagent
sequence tag identification
spin label
tag visualisation by dna adenine methyltransferase
transphenotypic genetic suppression
uniprot
uniprot knowledge base
uniprot/swiss-prot
uniprot/trembl
x-ray crystallography
MMO: Measurement Methods
arterial puncture
confocal microscopy
digital oral thermometry
ex vivo videomicroscopy
freezing point osmometry
inductively coupled plasma mass spectrometry
isolated bone method
manual oral thermometry
multiphoton microscopy
Na+ passive permeability assay in hypotonic choline medium
Na+ passive permeability assay in isotonic choline medium
Na+/K+ ATPase activity assay in hypotonic choline medium
Na+/K+ ATPase activity assay in isotonic choline medium
Na-K-Cl cotransport activity assay in hypotonic choline medium
Na-K-Cl cotransport activity assay in isotonic choline medium
venipuncture
MP: Mammalian Phenotype
abnormal adrenal gland zona intermedia morphology
abnormal adrenergic neuron morphology
abnormal anterior cerebral artery morphology
abnormal areal bone mineral density
abnormal astrocyte morphology
abnormal astrocyte number
abnormal asymmetric synapse morphology
abnormal auditory bulla morphology
abnormal azygos vein morphology
abnormal azygos vein topology
abnormal B cell morphology
abnormal B cell physiology
abnormal blood uric acid level
abnormal brachial lymph node morphology
abnormal brain external capsule morphology
abnormal brain interneuron morphology
abnormal cartilage development
abnormal cartilage morphology
abnormal cartilage physiology
abnormal cell nucleus morphology
abnormal cellular cementum morphology
abnormal cementoid morphology
abnormal centrosome morphology
abnormal cerebellar glomerulus morphology
abnormal cerebellar Golgi cell morphology
abnormal cerebellar granule layer morphology
abnormal cerebellum deep nucleus morphology
abnormal cerebellum dentate nucleus morphology
abnormal cerebellum emboliform nucleus morphology
abnormal cerebellum fastigial nucleus morphology
abnormal cerebellum lateral hemisphere morphology
abnormal cerebellum vermis lobule I morphology
abnormal cerebellum vermis lobule X morphology
abnormal cervical loop morphology
abnormal chorioallantoic fusion
abnormal choroid pigmentation
abnormal circulating estradiol level
abnormal circulating potassium level
abnormal circulating sodium level
abnormal circulating tyrosine level
abnormal clitoral bone morphology
abnormal clitoris size
abnormal coccyx morphology
abnormal cochlear IHC efferent innervation pattern
abnormal coronary sinus morphology
abnormal cranial vertex morphology
abnormal cremaster muscle morphology
abnormal cricoid cartilage morphology
abnormal dosage compensation
abnormal dosage compensation, by inactivation of X chromosome
abnormal eccrine gland number
abnormal eccrine sweat gland morphology
abnormal egg activation
abnormal epiglottis morphology
abnormal fat cell differentiation
abnormal fat cell morphology
abnormal fibrous joint morphology
abnormal forelimb morphology
abnormal fourth pharyngeal pouch morphology
abnormal fungiform papillae morphology
abnormal gastrocnemius morphology
abnormal gastrocnemius weight
abnormal gastrointestinal bezoar incidence
abnormal gastrointestinal lactobezoar incidence
abnormal gastrointestinal pharmacobezoar incidence
abnormal gastrointestinal phytobezoar incidence
abnormal gastrointestinal trichobezoar incidence
abnormal glycogen homeostasis
abnormal glycogen level
abnormal hair follicle infundibulum morphology
abnormal Harderian gland porphyrin secretion
abnormal head mesenchyme morphology
abnormal hindlimb morphology
abnormal hippocampal mossy fiber infrapyramidal bundle morphology
abnormal hippocampal mossy fiber innervation pattern
abnormal hippocampal mossy fiber morphology
abnormal hippocampal mossy fiber suprapyramidal bundle morphology
abnormal hippocampus CA2 region morphology
abnormal hippocampus CA3 region morphology
abnormal hippocampus CA4 region morphology
abnormal hyperactivated sperm motility
abnormal hypoglossal cord morphology
abnormal hypoglossal nucleus morphology
abnormal incisor morphology
abnormal inner hair cell stereociliary bundle morphology
abnormal intermediate gastric gland morphology
abnormal intestinal crypt stem cell morphology
abnormal intestinal crypt stem cell physiology
abnormal lamina terminalis morphology
abnormal lateral ganglionic eminence morphology
abnormal lens capsule morphology
abnormal Leydig cell differentiation
abnormal limb mesenchyme morphology
abnormal liver sinusoidal endothelial cell morphology
abnormal lower incisor morphology
abnormal lung-associated mesenchyme development
abnormal lymphocyte cell number
abnormal lymphocyte morphology
abnormal major salivary gland morphology
abnormal major salivary gland physiology
abnormal male prostatic urethra morphology
abnormal mast cell physiology
abnormal medial ganglionic eminence morphology
abnormal medulla oblongata morphology
abnormal Merkel's receptor morphology
abnormal mesenchyme morphology
abnormal mesoderm development
abnormal molar morphology
abnormal mucous gland morphology
abnormal nail matrix morphology
abnormal nasal fin morphology
abnormal navicular fossa morphology
abnormal olfactory bulb external plexiform layer morphology
abnormal olfactory bulb glomerular layer morphology
abnormal optic choroid morphology
abnormal optic fissure closure
abnormal optic tract morphology
abnormal outer hair cell stereociliary bundle morphology
abnormal palatal rugae morphology
abnormal parietal bone morphology
abnormal pectinate muscle morphology
abnormal penile bone morphology
abnormal periderm development
abnormal peritoneum morphology
abnormal pharyngeal arch mesenchyme morphology
abnormal piliary canal morphology
abnormal piriform aperture morphology
abnormal platelet alpha-granule morphology
abnormal platelet alpha-granule number
abnormal pluripotent precursor cell morphology
abnormal posterior cranial fossa morphology
abnormal presomitic mesoderm morphology
abnormal primordial germ cell morphology
abnormal proximal convoluted tubule morphology
abnormal pulmonary interalveolar septum morphology
abnormal sebocyte differentiation
abnormal sebocyte morphology
abnormal sebocyte physiology
abnormal skeletal muscle satellite cell proliferation
abnormal small intestine crypts of Lieberkuhn morphology
abnormal sphenoid sinus morphology
abnormal spleen red pulp morphology
abnormal stellate reticulum morphology
abnormal stomach smooth muscle outer longitudinal layer morphology
abnormal superior cerebellar peduncle morphology
abnormal synaptic norepinephrine release
abnormal tear film morphology
abnormal telencephalon development
abnormal telencephalon morphology
abnormal temporal bone petrous part morphology
abnormal temporalis muscle morphology
abnormal testis cord formation
abnormal tetrachloroethene metabolism
abnormal thalamus morphology
abnormal thalamus size
abnormal thermoreceptor morphology
abnormal touch/ nociception
abnormal type II hypersensitivity reaction
abnormal ultimobranchial body morphology
abnormal upper incisor morphology
abnormal upper rhombic lip morphology
abnormal urine uric acid level
abnormal uterine NK cell morphology
abnormal uterine NK cell physiology
abnormal vagal neural crest cell migration
abnormal ventral interneuron morphology
abnormal vibrissa morphology
abnormal vibrissa number
abnormal vitamin E level
abnormal volumetric bone mineral density
absent auditory bulla
absent B cells
absent brachial lymph nodes
absent cartilage
absent cerebellar granule layer
absent clitoral bone
absent coronary sinus
absent cricoid cartilage
absent eccrine glands
absent epiglottis
absent forelimb
absent fourth pharynegal pouch
absent head mesenchyme
absent hindlimb
absent incisors
absent lamina terminalis
absent lower incisors
absent lymphocyte
absent mesoderm
absent molars
absent optic tract
absent palatal rugae
absent parietal bone
absent pectinate muscle
absent primordial germ cells
absent segment of anterior cerebral artery
absent sternal manubrium
absent temporal bone petrous part
absent temporalis muscle
absent ultimobranchial body
absent upper incisors
absent uterine NK cells
absent vibrissae
alobar holoprosencephaly
aorta coarctation
cardiovascular shunt
carpoptosis
choroid inflammation
choroidal neovascularization
common atrioventricular valve
cranial bossing
craniorachischisis
curly vibrissae
decreased areal bone mineral density
decreased astrocyte number
decreased blood uric acid level
decreased brain external capsule size
decreased cerebellum dentate nucleus size
decreased circulating estradiol level
decreased circulating potassium level
decreased circulating sodium level
decreased cochlea coiling
decreased eccrine gland number
decreased fat cell size
decreased gastrocnemius weight
decreased glycogen level
decreased incisor number
decreased lymphocyte cell number
decreased molar number
decreased optic tract size
decreased palatal rugae number
decreased primordial germ cell number
decreased spleen red pulp amount
decreased susceptibility to type II hypersensitivity reaction
decreased thyroid gland lobe number
decreased urine uric acid level
decreased uterine NK cell number
decreased volumetric bone mineral density
delayed optic fissure closure
dilated piliary canal
ectopic kidney
ectopic neurohypophysis
ectopic pancreas
ectopic pregnancy
ectopic thyroid gland
encephalomeningocele
enlarged epiglottis
enlarged parietal bone
entropion
exostosis
glanular hypospadia
growth retardation of incisors
hyperinnervation of Merkel's receptor
hyperoxaluria
increased areal bone mineral density
increased astrocyte number
increased B cell acute lymphoblastic leukemia incidence
increased blood uric acid level
increased brain external capsule size
increased cardiac rhabdomyoma incidence
increased cerebellum dentate nucleus size
increased chronic lymphocytic leukemia incidence
increased circulating estradiol level
increased circulating gamma-glutamyl transferase level
increased circulating potassium level
increased circulating sodium level
increased cochlea coiling
increased eccrine gland number
increased fat cell size
increased gastrocnemius weight
increased glycogen level
increased lymphocyte cell number
increased Merkel's receptor number
increased optic tract size
increased osteochondroma incidence
increased primordial germ cell number
increased skin nevi incidence
increased spleen red pulp amount
increased susceptibility to type II hypersensitivity reaction
increased urine uric acid level
increased uterine NK cell number
increased vibrissae length
increased volumetric bone mineral density
kinked vibrissae
leukostasis
lobar holoprosencephaly
long incisors
long lower incisors
long upper incisors
loss of vibrissae
macrocytic anemia
macrodactyly
microcytic anemia
mosaic coat color
occipital vertebra
ostium primum atrial septal defect
patellar dislocation
peritoneal inflammation
persistent truncus arteriosus type iii
pharyngitis
piriform aperture stenosis
rachitic rosary
ruptured lens capsule
short incisors
short lower incisors
short parietal bone
short upper incisors
short vibrissae
sirenomelia
small brachial lymph nodes
small cricoid cartilage
small epiglottis
small incisors
small lower incisors
small molars
small parietal bone
small penile bone
small upper incisors
sparse vibrissae
spina bifida occulta
split sternal manubrium
supernumerary incisors
supernumerary molars
tangled vibrissae
thick pulmonary interalveolar septum
thin parietal bone
truncated digits
ureterocele
urethra obstruction
wavy vibrissae
Wormian bones
xanthoma
NBO: Neuro Behavioral Ontology
acute RBD
melancholic depression
selective mutism
OBA: Ontology of Biological Attributes
hippocampus mossy fiber morphology trait
PW: Pathway Ontology
aflatoxin metabolic pathway
altered cerebroside metabolic pathway
altered epidermal growth factor/neuregulin signaling pathway
altered glycosphingolipid metabolic pathway
altered sphingolipid metabolic pathway
Alzheimer's disease pathway
amyotrophic lateral sclerosis pathway
basal cell carcinoma pathway
bipolar disorder pathway
breast cancer pathway
carbon tetrachloride response pathway
catecholamine biosynthetic pathway
catecholamine degradation pathway
catecholamine metabolic pathway
CC chemokine mediated signaling pathway
Chagas disease pathway
chemokine mediated signaling pathway
cisplatin drug pathway
cisplatin response pathway
cocaine drug pathway
cocaine pharmacodynamics pathway
cortisol signaling pathway
Creutzfeldt-Jakob disease pathway
CXC chemokine mediated signaling pathway
deoxyribonucleotide metabolic pathway
dilated cardiomyopathy pathway
erythromycin biosynthetic pathway
estradiol biosynthetic pathway
ethylmorphine drug pathway
fatty acid beta degradation pathway
Fc gamma receptor mediated signaling pathway
gastric cancer pathway
glucose homeostasis pathway
heparan sulfate biosynthetic pathway
heparan sulfate metabolic pathway
Huntington's disease pathway
inositol metabolic pathway
interleukin-33 signaling pathway
isoprenoid metabolic pathway
Leishmaniasis pathway
lipoid congenital adrenal hyperplasia pathway
lung cancer pathway
malaria pathway
mitochondrial protein import pathway
mitochondrial translation pathway
N-acetylglucosamine, N-acetylmannosamine and N-acetylneuraminic acid dissimilation pathway
non-homologous end joining pathway of double-strand break repair
nuclear factor, erythroid 2 like 2 signaling pathway
orotic aciduria 1 pathway
oxaliplatin drug pathway
parathyroid hormone-like hormone signaling pathway
Parkinson's disease pathway
phenylketonuria pathway
platinum (Pt) containing drug response pathway
prostaglandin E2 signaling pathway
pyrimidine salvage pathway
radical SAM enzyme mediated RNA processing pathway
Staphylococcus aureus infection pathway
sulfate assimilation pathway
tamoxifen drug pathway
thyroid cancer pathway
toxoplasmosis pathway
translation initiation pathway
triacylglycerol biosynthetic pathway
tuberculosis pathway
tuberoinfundibular 39 residues peptide signaling pathway
vascular endothelial growth factor signaling pathway
RDO: RGD Disease Ontology
45,X/46,XY mixed gonadal dysgenesis
Abdominal Fibromatosis
Acne Keloid
acoustic neuroma
Acrodynia
acute diarrhea
Acute Generalized Exanthematous Pustulosis
acute interstitial pneumonia
agnathia-otocephaly complex
Aicardi-Goutieres syndrome
AIDS-Related Opportunistic Infections
Alcohol Withdrawal Seizures
Alice in Wonderland Syndrome
alpha-gal syndrome
Alpha-Mannosidosis, Type 2
Alternating Hemiplegia of Childhood 1
Alternating Hemiplegia of Childhood 2
amyotrophic lateral sclerosis type 1
Anastomotic Leak
apolipoprotein A-IV associated amyloidosis
Arachnoid Cysts
arachnoiditis
Arbovirus Encephalitis
Arnold-Chiari Malformation
asymptomatic dengue
autosomal dominant intellectual developmental disorder 56
autosomal dominant osteopetrosis 1
Autosomal Recessive Peripheral Neuropathy with or without Impaired Intellectual Development
Avian Leukosis
Avulsion Fractures
Bacteremia
Barmah Forest virus disease
Becker Nevus Syndrome
benign recurrent intrahepatic cholestasis
bile duct carcinoma in situ
blastic plasmacytoid dendritic cell neoplasm
Blastocystis Infections
Bloch-Sulzberger syndrome
Bone Marrow Neoplasms
bone osteosarcoma
Bowen's Disease
Brain Hypoxia
Bronchial Hyperreactivity
bronchopulmonary dysplasia
bronchus carcinoma in situ
Buruli ulcer disease
Calculi
candidal paronychia
candidiasis
carotid stenosis
Carpenter syndrome 2
Central Centrifugal Cicatricial Alopecia
Central Nervous System Venous Angioma
central neurocytoma
Cerebrospinal Fluid Leak
Chagas Cardiomyopathy
Chagas disease
chikungunya
chondromyxoid fibroma
Choroid Neoplasms
Choroid Plexus Neoplasms
choroid plexus papilloma
chromoblastomycosis
Chromosome 1, Uniparental Disomy 1q12 q21
Chromosome 10, Uniparental Disomy of
Chromosome 13q-Mosaicism
Chromosome 14, Trisomy Mosaic
Chromosome 15 Ring
Chromosome 15, Trisomy Mosaicism
Chromosome 16, Trisomy
Chromosome 17 Trisomy
Chromosome 18 Mosaic Monosomy
Chromosome 20, Trisomy
Chromosome 21, Uniparental Disomy of
Chromosome 22, Monosome Mosaic
Chromosome 5, Uniparental Disomy
Chromosome 7, Trisomy Mosaic
Chromosome 8, Mosaic Trisomy
Chromosome 9, Tetrasomy 9p
Chromosome 9, Trisomy Mosaic
Chronic Exertional Compartment Syndrome
Chronic Periodontitis
chronic urticaria
Classical Lissencephalies and Subcortical Band Heterotopias
CLOVES syndrome
common wart
congenital central hypoventilation syndrome
congenital disorder of glycosylation It
Congenital Heart Defects, Multiple Types, 9
Congenital Hyperinsulinism
congenital nonspherocytic hemolytic anemia 1
CONGENITAL SMOOTH MUSCLE HAMARTOMA, WITH OR WITHOUT HEMIHYPERTROPHY
Contrecoup Injury
conventional osteosarcoma
Corneal Graft Rejection
coronary aneurysm
CRANIAL DYSINNERVATION DISORDER, CONGENITAL, WITH ABSENT CORNEAL REFLEX AND DEVELOPMENTAL DELAY
Craniomandibular Disorders
Creutzfeldt-Jakob disease
cutaneous mastocytosis
Cytomegalovirus Infections
D-bifunctional protein deficiency
Delayed Graft Function
dengue disease
dengue hemorrhagic fever
dengue shock syndrome
Dentigerous Cyst
desmoid tumor
desmoplastic small round cell tumor
developmental and epileptic encephalopathy 56
DEVELOPMENTAL DELAY WITH VARIABLE NEUROLOGIC AND BRAIN ABNORMALITIES
DEVELOPMENTAL DELAY, BEHAVIORAL ABNORMALITIES, AND NEUROPSYCHIATRIC DISORDERS
DEVELOPMENTAL DELAY, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES, WITH OR WITHOUT SEIZURES
Diaper Rash
diarrhea
Digital Dermatitis
dipetalonemiasis
Diploid-Triploid Mosaicism
dirofilariasis
Disease Progression
Disease Resistance
Diseases of the Aged
Drug-Induced Dyskinesia
Ductal, Lobular, and Medullary Neoplasms
Dupuytren Contracture
Eastern equine encephalitis
eccrine acrospiroma
eccrine porocarcinoma
ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES
Edema
Edwards syndrome
embryonal rhabdomyosarcoma
Endocrine Tuberculosis
endomyocardial fibrosis
Enteropathy-Associated T-Cell Lymphoma
Enzootic Pneumonia of Calves
Eosinophilic Granuloma
eosinophilic pneumonia
Ependymomas
Epidermitis, Exudative, of Swine
epidermolysis bullosa simplex Dowling-Meara type
epidural spinal canal neoplasm
epiglottitis
Epilepsia Partialis Continua
Epithelioid Leiomyoma
Equine Encephalomyelitis
erysipelas
Erythema Induratum
Erythropoietic Protoporphyria 1
Esophageal Fistula
Esophageal Stenosis
essential hypertension
euthyroid sick syndrome
Experimental Autoimmune Neuritis
Familial Hemophagocytic Lymphohistiocytoses
Familial Partial Lipodystrophy Type 9
Fibromuscular Dysplasia
filarial elephantiasis
Fistula
Fontaine Progeroid Syndrome
Foodborne Diseases
Foveal Hypoplasia 3
Friedreich ataxia
Fungemia
GABA aminotransferase deficiency
Galactorrhea
gallbladder carcinoma in situ
Galloway-Mowat Syndrome 6
generalized dystonia
Generalized Epilepsy with Febrile Seizures Plus, Type 12
Giant Cell Carcinoma
Giant Cell Tumors
glioblastoma mesenchymal subtype
GLOBAL DEVELOPMENTAL DELAY WITH SPEECH AND BEHAVIORAL ABNORMALITIES
Global Developmental Delay, Lung Cysts, Overgrowth, and Wilms Tumor
glomangioma
Glycosylphosphatidylinositol Biosynthesis Defect 15
gnathomiasis
granular cell tumor
Hailey-Hailey disease
Heat Stroke
hemangioblastoma
Hennekam syndrome
Hereditary Hemorrhagic Telangiectasia, Type 1
high-grade astrocytoma with piloid features
Hydatidiform Mole, Invasive
hypercementosis
Hyperhidrosis
Hyperkalemia
Hyperostosis Frontalis Interna
Hypertensive Intracranial Hemorrhage
ileocolitis
immature teratoma of ovary
immunodeficiency-centromeric instability-facial anomalies syndrome
Infarction
intellectual developmental disorder with autistic features and language delay, with or without seizures
Intellectual Developmental Disorder with Dysmorphic Facies and Ptosis
INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD
INTELLECTUAL DEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND EARLY-ONSET DOPA-RESPONSIVE DYSTONIA-PARKINSONISM
INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, WITH PIGMENTARY MOSAICISM AND COARSE FACIES
Intervertebral Disc Displacement
intestinal atresia
intracranial aneurysm
intracranial berry aneurysm
intracranial embolism
Intradermal Nevus
Invasive Breast Carcinoma
Invasive Candidiasis
Iridocorneal Endothelial Syndrome
iron metabolism disease
ischemic cardiomyopathy
Isolated Systolic Hypertension
Japanese encephalitis
Karoshi Death
Kidney Calculi
Kimura disease
Kunjin encephalitis
kuru
KURY-ISIDOR SYNDROME
La Crosse encephalitis
Labor Pain
Landau-Kleffner syndrome
laryngomalacia
Leber congenital amaurosis 4
leiomyosarcoma
leukostasis
linear nevus sebaceous syndrome
linitis plastica
Lithiasis
Lyme Neuroborreliosis
lymphoid interstitial pneumonia
macular retinal edema
malaria
malignant fibrous histiocytoma
malignant fibrous histiocytoma of bone
Marshall syndrome
MCD diffuse large B-cell lymphoma
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 5
melorheostosis
Mental Retardation, Autosomal Recessive 53
Merkel cell carcinoma
Mesonephroma
Microcephaly, Facial Dysmorphism, Renal Agenesis, and Ambiguous Genitalia Syndrome
Morbid Obesity and Spermatogenic Failure
mosaic variegated aneuploidy syndrome
mosaic variegated aneuploidy syndrome 1
mosaic variegated aneuploidy syndrome 2
mosaic variegated aneuploidy syndrome 3
mosaic variegated aneuploidy syndrome 4
Mosaic Variegated Aneuploidy Syndrome 5
Mosaic Variegated Aneuploidy Syndrome 6
mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition
mucinous cystadenocarcinoma of pancreas
Mucinous Cystadenoma
Mucoepidermoid Tumor
MUGGENTHALER-CHOWDHURY-CHIOZA SYNDROME
multidrug-resistant tuberculosis
Multiple Exostoses Type I
Multiple Exostoses Type II
Murray Valley encephalitis
muscular dystrophy-dystroglycanopathy type B
myeloid and lymphoid neoplasms associated with PDGFRA rearrangement
myeloid and lymphoid neoplasms associated with PDGFRB rearrangement
myoclonic dystonia
myoclonic dystonia 11
myopathy with extrapyramidal signs
necrotizing fasciitis
Neonatal Sepsis
nephrotic syndrome type 3
Nervous System Lead Poisoning, Adult
Nervous System Lead Poisoning, Childhood
Neurocysticercosis
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS
Neurodevelopmental Disorder with Impaired Speech and Hyperkinetic Movements
NEURODEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT, AUTISM, AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER
NEURODEVELOPMENTAL DISORDER WITH NEUROMUSCULAR AND SKELETAL ABNORMALITIES
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES
neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND BRAIN ATROPHY
neurofibrosarcoma
neuronal ceroid lipofuscinosis 6A
NEUROOCULAR SYNDROME 2, PAROXYSMAL TYPE
Nevus, Epithelioid and Spindle Cell
nodular nonsuppurative panniculitis
non-syndromic X-linked intellectual disability 46
NUT midline carcinoma
O'nyong-nyong fever
oculoectodermal syndrome
Odontodysplasia
oligoasthenoteratozoospermia
oligodendroglioma
Oocyte/Zygote/Embryo Maturation Arrest 20
optic nerve neoplasm
oral cavity carcinoma in situ
orbit rhabdomyosarcoma
ossifying fibromyxoid tumor
Osteochondroma
Osteoid Osteoma
otomycosis
otopalatodigital syndrome spectrum disorder
Ovarian Granulosa Cell Tumor
Ovotesticular Disorders of Sex Development
Pallister Killian Syndrome
pancreatic intraductal papillary-mucinous neoplasm
Pancreatic Pseudocyst
Panniculitis, Lupus Erythematosus
Papulosquamous Skin Diseases
Paralysis
paraneoplastic polyneuropathy
paraplegia
Parasitic Lung Diseases
parosteal osteosarcoma
partial fetal alcohol syndrome
patellofemoral pain syndrome
Peritoneal Carcinomatosis
Phelan-McDermid syndrome
Pinealoma
pituitary apoplexy
plaque psoriasis
Pneumococcal Meningitis
podoconiosis
POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME
Polyarteritis Nodosa, Childhood-Onset
polycystic kidney disease 6
pontocerebellar hypoplasia type 1E
PORETTI-BOLTSHAUSER SYNDROME
Porokeratosis 6, Multiple Types
Porokeratosis, Disseminated Superficial Actinic, 3
Porokeratosis, Disseminated Superficial Actinic, 4
Porokeratosis, Disseminated Superficial Actinic, 8
Port-Wine Stain
posterior amorphous corneal dystrophy
Posterior Tibial Tendon Dysfunction
posterior uveitis
Preauricular Tag, Isolated, Autosomal Dominant, 1
Presumed Ocular Histoplasmosis Syndrome
Primary Effusion Lymphoma
Primary Graft Dysfunction
PRIMORDIAL DWARFISM-IMMUNODEFICIENCY-LIPODYSTROPHY SYNDROME
prostate embryonal rhabdomyosarcoma
prostatic acinar adenocarcinoma
Proteus syndrome
Psoas Abscess
pulmonary blastoma
pulmonary embolism and infarction
pyoderma gangrenosum
rabies
Recurrent Metabolic Crises with Variable Encephalomyopathic Features and Neurologic Regression
reflex sympathetic dystrophy
Renal Colic
Renal Hypodysplasia/Aplasia 1
Renal Hypodysplasia/Aplasia 3
renal oncocytoma
Renpenning syndrome
ReNU syndrome
Reperfusion Injury
restrictive dermopathy
reticular dysgenesis
Reticulocytosis
retinitis pigmentosa 96
Rheumatic Nodule
Rheumatoid Nodule
Rift Valley fever
Roseolovirus Infections
Ross River fever
rumination disorder
salmonellosis
Scleromyxedema
sclerosteosis
Sclerotylosis
Sd(a) POLYAGGLUTINATION SYNDROME
sebaceous adenocarcinoma
seborrheic keratosis
secretory diarrhea
Seroma
Serotonin Syndrome
serous labyrinthitis
Sex Chromosome Disorders of Sex Development
sialolithiasis
skin amelanotic melanoma
Slipped Capital Femoral Epiphyses
Smoke Inhalation Injury
Solitary Fibrous Tumors
Sphincter of Oddi Dysfunction
spinal cancer
Spinal Cord Neoplasms
spinal muscular atrophy with lower extremity predominant
spondyloarthropathy
St. Louis encephalitis
status epilepticus
Stolerman neurodevelopmental syndrome
Stress Fractures
Subarachnoid Hemorrhage
SULFIDE:QUINONE OXIDOREDUCTASE DEFICIENCY
Sunstroke
syndromic microphthalmia 2
Synesthesia
Synovial Cyst
syringoma
syringomyelia
Talipes
TDP-43 Proteinopathies
telangiectasis
Tendon Entrapment
Thecoma
Thrombotic Microangiopathies
thrombotic thrombocytopenic purpura
Thrombotic Thrombocytopenic Purpura, Acquired
thunderstorm triggered asthma
tibial neuropathy
Tonne-Kalscheuer syndrome
toxoplasmosis
transient neonatal diabetes mellitus
tricuspid valve prolapse
Trigeminal Autonomic Cephalalgias
Trisomy 22 Mosaicism Syndrome
Tubal Pregnancy
tubulinopathy
typhus
uremia
urticaria pigmentosa
USMANI-RIAZUDDIN SYNDROME, AUTOSOMAL DOMINANT
USMANI-RIAZUDDIN SYNDROME, AUTOSOMAL RECESSIVE
uveal cancer
Vascular Malformations
velocardiofacial syndrome
Venezuelan equine encephalitis
Ventricular Premature Complexes
Ventricular Remodeling
Veterinary Venereal Tumors
vipoma
Viral Bronchiolitis
Viral Hemorrhagic Fevers
visceral leishmaniasis
vitamin K deficiency bleeding
West Nile encephalitis
West Nile fever
Western equine encephalitis
White Muscle Disease
Wilms Tumor 6
yellow fever
Zika fever
RS: Rat Strains
WMI/EerRrrc
SO: Sequence Ontology
C_D_box_snoRNA
C_D_box_snoRNA_gene
cytosolic_25S_rRNA
five_prime_clip
five_prime_coding_exon
five_prime_intron
H_ACA_box_snoRNA
H_ACA_box_snoRNA_gene
interior_coding_exon
interior_intron
isomiR
major_TSS
minor_TSS
modified_L_serine
Mutator_TIR_transposon
noncontiguous_finished
polyA_sequence
SL1_acceptor_site
SRP_RNA
TCT_motif
three_prime_clip
three_prime_coding_exon
three_prime_intron
wobble_base_pair
X_element
UBERON: Cross-Species Anatomy
abdominal external oblique muscle
accessory nerve cord of dorsal region
acetabular depression
adult mammalian kidney
akrokranion
alular digit
amphicoelous
ampulla of fallopian tube
ampulla of Lorenzini
antenna
anterior articular facet for talus of calcaneus
anterior cerebral artery
anterior jugular vein
anterior lateral line
anterior lateral line system
anterior nuclear group
anterior root of zygomatic arch
anterior tibial vein
anterior ventrolateral plate
anterior wall of urinary bladder
antimesosalpinx-proximal fallopian tube epithelium
antimesosalpinx-proximal muscular layer of fallopian tube
antler
arciferal girdle
auditory bulla
azygos vein
basicranium
basihyal bone
basihyal cartilage
basihyal element
basioccipital bone
biceps brachii
biliary system
brachial lymph node
brain
branchiostegal ray
branchiostegal ray 1
branchiostegal ray 2
branchiostegal ray 3
Brodmann (1909) area 10
Brodmann (1909) area 12
Brodmann (1909) area 16
Brodmann (1909) area 20
Brodmann (1909) area 21
Brodmann (1909) area 32
Brodmann (1909) area 35
Brodmann (1909) area 38
Brodmann (1909) area 46
buccal vestibule
C lamina of the lateral geniculate nucleus (sensu Mustela putorius furo)
C1 segment of cervical spinal cord
C2 segment of cervical spinal cord
C3 segment of cervical spinal cord
C4 segment of cervical spinal cord
C5 segment of cervical spinal cord
C6 segment of cervical spinal cord
C7 segment of cervical spinal cord
C8 segment of cervical spinal cord
CA2 field of hippocampus
CA3 field of hippocampus
CA4 field of hippocampus
camptotrichium
capsule of lens
cardiac jelly
carpometacarpus
cartilaginous neurocranium
cauda equina
caudal fin
caudal part of nephrogenic cord
caudofemoralis
celiac ganglion
central carpal bone
centrale 1
centrale 2
ceratobranchial 5 bone
ceratobranchial 5 cartilage
cerebellar glomerulus
cerebellar hemisphere
cerebellar nuclear complex
cerebellar vermis
chorionic terminal villus
chromaffin paraganglion
ciliary marginal zone
clavotrapezius muscle
clivus of occipital bone
colon
coprodeum
coracoid process of scapula
coronary sinus
corpus cavernosum clitoridis
cortical layer I
cremaster muscle
cuneus cortex
dense regular connective tissue
dentate gyrus polymorphic layer
dentate nucleus
distal carpal bone 5
distal phalanx
distal-most prehallical element
distal-most prepollical element
dorsal motor nucleus of vagus nerve
dorsal ocellus
dorsal pes interosseous muscle
dorsolateral prefrontal cortex layer 1
duct of eccrine sweat gland
ductus arteriosus
ectopterygoid bone
ectorbitale
emboliform nucleus
embryonic cement gland
endomysium
endoskeletal cranial joint
entire pharyngeal arch associated mesenchyme
entorhinal cortex layer 1
epiglottic cartilage
epineural
epithalamus
ethmoid region
euryon
external capsule of telencephalon
external gill
fastigial nucleus
fibularis longus
filiform papilla
flexural organ
forebrain
forelimb epitrochlearis muscle
fourth phalanx
frontal lobe
fundus of gallbladder
fungiform papilla
ganglion
gastrocnemius
gastrula stage
gluteus maximus
gracilis
granular layer of cerebellar cortex
habenular trigone
hair canal
head
head mesenchyme
headfoot
helicine branch of uterine artery
hemal postzygapophysis
hemolymph
hilum of inferior olivary complex
hindbrain
hippocampus molecular layer
hippocampus stratum lucidum
hyohyoideus
hyomandibular element
hypoconid
hypothalamus
ileal branch of ileocolic artery
ilium
inferior muscular layer of fallopian tube
inner digits of foot
inner digits of hand
insect abdomen
insect embryonic/larval lymph gland
insect labial segment
insect metathoracic segment
insect prothoracic segment
insect protocerebrum
insect tarsal segment
insect tracheal pit
intermediate gastric gland
interstitial nucleus of Cajal
interthalamic adhesion
intestinal bulb
intromittent organ
isla magna of Calleja
knee joint
Kupffer's vesicle
L1 segment of lumbar spinal cord
L2 segment of lumbar spinal cord
L3 segment of lumbar spinal cord
L4 segment of lumbar spinal cord
L5 segment of lumbar spinal cord
lamina anterior of maxilla
lamina terminalis of neural tube
lateral extrascapular
lateral ganglionic eminence
lateral line
layer of dura mater
limb mesenchyme
lingual gyrus
longissimus thoracis muscle
lower lobe of lung
lymph node paracortex
lymphoid tissue
magnocellular reticular nucleus
major salivary gland
mammalian cervical vertebra 7
mandible coronoid process
mandibular arch neural crest
manubrium of sternum
meandering mesenteric artery
medial forebrain bundle
medial ganglionic eminence
medial nucleus of trapezoid body
medial rectus extraocular muscle
median dorsal plate
median ventricular nerve (sensu Cancer borealis)
meningeal dura mater
mesenteric artery
mesosalpinx-proximal fallopian tube epithelium
mesosalpinx-proximal muscular layer of fallopian tube
metacarpus skeleton
metanephric mesenchyme
metanephric proximal convoluted tubule
middle colic artery
molar tooth
mossy fiber
moustache
mucosa
mucus body coating
muscularis mucosa
nasal artery
nasal bone
nasal fin
nasal vestibule
navicular fossa of spongiose part of urethra
neocortex
nidopallium
notochord
nucleus raphe magnus
olfactory bulb external plexiform layer
olfactory bulb glomerular layer
operculum of brain
opisthocoelous
oral gland
orbital margin
os clitoris
os penis
otion
ovary stroma
P1 area of pallium (Myxiniformes)
P5 area of pallium (Myxiniformes)
paramedian reticular nucleus
parapodium
parasympathetic nervous system
parietal organ
parieto-occipital sulcus
pectinate muscle
pectoantebrachialis
pectoral fin proximal radial element 1
pectoral fin proximal radial element 2
pectoral fin proximal radial element 3
pectoral fin proximal radial element 4
pectoral fin ray 2
pectoral fin ray 3
pectoral fin ray 4
pectoral fin ray 5
pectoral fin ray 6
pectoral fin ray 7
pectoral fin spine
pennaceous feather
pericalcarine cortex
petrous part of temporal bone
pharyngeal nerve plexus
pharyngobranchial 1 bone
pharyngobranchial 1 cartilage
pharyngobranchial 1 element
pharyngobranchial 4 bone
pharyngobranchial 4 cartilage
pharyngobranchial 4 element
piriform aperture
piriform cortex layer 1
planum temporale
portal system
postcleithrum 1
posterior articular facet for talus of calcaneus
posterior commissure
posterior lateral line system
posterior tibial vein
posterior ventrolateral plate
posterior wall of the glottis
posterior wall of urinary bladder
posttemporal fossa
prefrontal cortex
preganglionic autonomic fiber
preglomerular nucleus
presomitic mesoderm
presumptive hindbrain
primary dorsal nerve cord
primary nerve cord
primary olfactory cortex
primary ossification center
principal sensory nucleus of trigeminal nerve
prismatic cartilage
procoelous
proctodeum portion of cloaca
prostatic urethra
prosthion
proximal convoluted tubule
proximal mesopodial endochondral element
proximal phalanx
proximal-most point of greater trochanter of femur
proximal-most point of head of femur
proximal-most point of head of humerus
proximal-most point of ventral tubercle of humerus
proximal-most prehallical element
proximal-most prepollical element
putamen
quadratojugal bone
red nucleus
red pulp of spleen
renin-angiotensin system
reticulotegmental nucleus
roofing cartilage
rostral part of nephrogenic cord
S1 segment of sacral spinal cord
S2 segment of sacral spinal cord
S3 segment of sacral spinal cord
S4 segment of sacral spinal cord
S5 segment of sacral spinal cord
sacral nerve plexus
saphenous artery
scalenus posterior
scent gland
sclerotome
second phalanx
secondary ossification center
secondary prosencephalon
semimembranosus muscle
septohippocampal nucleus
shoulder bone
spinotrapezius muscle
squamous epithelium
stellate vein of kidney
stomach smooth muscle outer longitudinal layer
strand of guard hair
strand of hair
strand of vibrissa hair
subarticular sesamoid
subarticular tubercles
submandibular lymph node
suborbital stay
substantia nigra
superficial fascia
superior colliculus stratum zonale
superior laryngeal nerve
superior muscular layer of fallopian tube
surangular bone
sympathetic nervous system
synarthrosis
synovial bursa
T1 segment of thoracic spinal cord
T10 segment of thoracic spinal cord
T11 segment of thoracic spinal cord
T12 segment of thoracic spinal cord
T2 segment of thoracic spinal cord
T3 segment of thoracic spinal cord
T4 segment of thoracic spinal cord
T5 segment of thoracic spinal cord
T6 segment of thoracic spinal cord
T7 segment of thoracic spinal cord
T8 segment of thoracic spinal cord
T9 segment of thoracic spinal cord
tertiary ovarian follicle
thermoreceptor
thoracic skeleton
tibialis posterior
trabecula
transition zone of prostate
transverse folds of rectum
transverse palatine fold
trochlea of humerus
turtle shell
tympanic ring
upper rhombic lip
ural centrum
uterine tube magnum
vellus hair
ventral ridge system
ventral striatum
Virchow's lymph node
visceral hump
vitelline membrane
xiphihumeralis
zygion
VT: Vertebrate Trait Ontology
adipose beta-carotene amount
biceps brachii muscle mass
blood ceruloplasmin amount
blood cholesterol amount
blood estradiol amount
blood immunoglobulin M amount
blood potassium amount
blood sodium amount
brachial lymph node morphology trait
brachial lymph node size trait
brain cholesterol amount
brain interneuron morphology trait
cartilage development trait
cartilage molecular composition trait
cartilage morphology trait
cartilage ribonucleic acid amount
cerebellar glomerulus morphology trait
cerebellar granule layer morphology trait
cholesterol absorption trait
cholesterol amount
cholesterol homeostasis trait
chorioallantoic fusion trait
choroid morphology trait
choroid pigmentation trait
cochlear inner hair cell efferent nerve fiber organization trait
cochlear inner hair cell efferent nerve fiber quantity
cochlear outer hair cell stereociliary bundle morphology trait
cricoid cartilage morphology trait
epiglottis morphology trait
erythrocyte sodium amount
estrus intensity
forebrain 5-hydroxyindoleacetic acid amount
forebrain cell quantity
forebrain development trait
forebrain dihydroxyphenylacetic acid (DOPAC) amount
forebrain dopamine amount
forebrain epinephrine amount
forebrain homovanillic acid amount
forebrain morphology trait
forebrain norepinephrine amount
forebrain serotonin amount
fungiform papillae morphology trait
gastrocnemius molecular composition trait
gastrocnemius morphology trait
hippocampus mossy fiber morphology trait
hypoglossal nucleus morphology trait
incisor growth trait
incisor morphology trait
inner hair cell stereociliary bundle morphology trait
larynx morphology trait
lateral ganglionic eminence morphology trait
limb joint molecular composition trait
limb joint morphology trait
liver cholesterol amount
major salivary gland morphology trait
mast cell physiology trait
medial ganglionic eminence morphology trait
medulla oblongata dopamine amount
medulla oblongata morphology trait
Merkel's receptor morphology trait
Merkel's receptor nerve fiber organization trait
Merkel's receptor nerve fiber quantity
Merkel's receptor quantity
mesenteric artery morphology trait
mesenteric artery ribonucleic acid amount
milk alpha-S1-casein amount
milk beta-carotene amount
milk immunoglobulin M amount
molar growth trait
molar morphology trait
muscle arsenic amount
muscle cholesterol amount
muscle glycogen homeostasis trait
muscle zinc amount
neural plate morphology trait
pluripotent precursor cell morphology trait
retroperitoneal fat pad mass
retroperitoneal fat pad morphology trait
semimembranosus mass
semimembranosus size trait
semimembranosus width
skeletal muscle myosin heavy chain type I amount
skeletal muscle myosin heavy chain type IIa amount
skeletal muscle myosin heavy chain type IIb amount
skin sodium amount
sphenoid bone morphology trait
spleen red pulp morphology trait
synaptic norepinephrine release trait
temporalis muscle morphology trait
temporalis muscle size trait
thalamus cell quantity
thalamus morphology trait
thermoreceptor morphology trait
ultimobranchial body morphology trait
XCO: Experimental Condition
3D printed β‐TCP scaffold implantation
alpha-tocopherol
anti-RT6.1 antibody
bacteria
caffeine
crystalline silica
diestrus
double-distilled water
duodenal-jejunal bypass
fetal bovine serum
gastric bypass
Helicobacter pylori
leg-out partial body irradiation
lipopolysaccharide
megestrol
morphine
nitrofurantoin
ochratoxin A
ovalbumin
parasite behavior in a Skinner box within a worker/parasite group feeding/reward paradigm
pertussis toxin
room temperature
spinal nerve ligation
streptococcal cell wall
vasopressin
vitamin C
worker behavior in a Skinner box within a worker/parasite group feeding/reward paradigm
PathwaysPathways with diagrams.mitochondrial protein import pathway fatty acid beta degradation pathway estradiol biosynthetic pathway Parkinson disease pathway Huntington disease pathway Alzheimer's disease pathway cisplatin response pathway non-homologous end joining pathway of double-strand break repair vascular endothelial growth factor signaling pathway cisplatin drug pathway nuclear factor, erythroid 2 like 2 signaling pathway cortisol signaling pathway |
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