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Ontology Browser

Vascular Hyalinosis (DOID:9004811)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
diarrhea +     
intestinal disease +     
Skin Abnormalities +     
vascular disease +     
4-Hydroxyphenylacetic Aciduria 
achromatopsia 4  
Achromatopsia 5  
acrodermatitis +   
Acrootoocular Syndrome 
acute diarrhea 
acute vascular insufficiency of intestine 
Aicardi syndrome 
Alacrima +   
Albinism +   
Anetoderma +   
Aneurysm +   
angiodysplasia +   
angiodysplasia of intestine 
angioedema +   
Angiomatosis +   
angiomyoma +  
aniridia +   
anterior ischemic optic neuropathy +   
Arterial Dissection with Lentiginosis 
Arterial Injury +   
Arterial Occlusive Diseases +   
arteriovenous malformation +   
artery disease +   
ataxia with oculomotor apraxia type 3  
Ataxia-Microcephaly-Cataract Syndrome 
Ataxia-Oculomotor Apraxia 4  
Autoinflammation with Arthritis and Dyskeratosis  
Barber-Say syndrome  
basal laminar drusen  
Beare-Stevenson cutis gyrata syndrome  
Bile Acid Malabsorption, Primary  
Blepharophimosis with Ptosis, Syndactyly, and Short Stature 
blepharophimosis, ptosis, and epicanthus inversus syndrome +   
Bloch-Sulzberger syndrome +   
Book Syndrome 
Bothnia retinal dystrophy  
bowel dysfunction +   
C1q Deficiency  
capillary disease +   
Carney complex +   
Carotid Intimal Medial Thickness 2 
cataract 17 multiple types  
cataract 22 multiple types  
cataract 35 
Cataract, Floriform 
Cataract, Pulverulent 
Cavitary Optic Disc Anomalies  
cecal disease +   
cerebrovascular disease +   
Cholestasis with Gallstone, Ataxia, and Visual Disturbance 
cholesterol embolism +   
Choroideremia +   
Chronic Diarrhea with Villous Atrophy 
chronic intestinal vascular insufficiency 
colonic disease +   
compartment syndrome +   
cone-rod dystrophy +   
Congenital Alacrima +   
congenital diarrhea +   
Congenital Fibrosis of Extraocular Muscles, 2  
Congenital Fibrosis of Extraocular Muscles, 3A, with or without Extraocular Involvement  
Congenital Fibrosis of Extraocular Muscles, 3B  
Congenital Fibrosis of Extraocular Muscles, 3C 
Congenital Fibrosis of Extraocular Muscles, 5  
Congenital Mydriasis +   
Cornea Plana 1 
Cornea Plana 2  
corneal dystrophy +   
Cronkhite-Canada syndrome +   
Cutaneous Hemangiomatosis with Associated Features 
Dermal Ridges, Nelson Syndrome 
diverticulitis +   
Drug-Induced Enteropathy +   
Duane retraction syndrome +   
duodenum disease +   
dysentery +   
dyskeratosis congenita +   
ectodermal dysplasia +   
Ehlers-Danlos syndrome +   
Embolism and Thrombosis +   
endometriosis of intestine 
enhanced S-cone syndrome  
Enteritis +   
Enterocolitis +   
enterokinase deficiency  
epidermolysis bullosa +   
Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract 
Erosive Arthropathy 
exudative vitreoretinopathy +   
familial benign fleck retina  
Familial Dyskeratotic Comedones 
Familial Popliteal Pterygium Syndrome 
fetal encasement syndrome  
Foveal Hypoplasia +   
Foveal Hypoplasia with Anterior Segment Anomalies 
functional diarrhea 
Glaucoma 1, Open Angle, P  
Graves Ophthalmopathy  
Grouped Pigmentation of the Macula 
gyrate atrophy +   
Hairy Palms and Soles 
Hand-Arm Vibration Syndrome 
hepatic vascular disease +   
hereditary arterial and articular multiple calcification syndrome +   
Hereditary Benign Intraepithelial Dyskeratosis 
hereditary night blindness +   
Hereditary Optic Atrophies +   
hereditary retinal dystrophy +   
Hereditary Sclerosing Poikiloderma +   
high hyperopia  
Histiocytic Dermatoarthritis 
HIV Enteropathy 
Homozygous 11p15-p14 Deletion Syndrome 
Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated with Cerebral Capillary Malformations  
hypertension +   
Hypohidrosis with Abnormal Palmar Dermal Ridges 
Hypotension +   
ichthyosis +   
Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 
Ileal Diseases +   
Infantile Cataract, Skin Abnormalities, Glutamate Excess, and Impaired Intellectual Development  
Infantile Diarrhea +   
inflammatory bowel disease +   
inflammatory diarrhea 
inguinal hernia +   
intestinal atresia +   
intestinal disaccharidase deficiency 
Intestinal Fistula +   
intestinal infectious disease +   
Intestinal Ischemia +   
Intestinal Neoplasms +   
intestinal obstruction +   
intestinal perforation +   
intestinal schistosomiasis +   
intestinal tuberculosis 
intravenous leiomyomatosis 
Iris Pigment Epithelium Anomalies 
ischemia +   
ischemic colitis  
Isolated Pterygium Colli 
Jejunal Diseases +  
Joubert syndrome 8  
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
Leber congenital amaurosis +   
lethal restrictive dermopathy  
Malabsorption Syndromes +   
male genital organ vascular disease 
megalocornea +   
Mesenteric Ischemia  
mesenteric vascular occlusion  
Microcephaly and Chorioretinopathy +   
MLS syndrome +   
motility-related diarrhea 
mucocele of appendix 
multiple benign circumferential skin creases on limbs +   
multiple pterygium syndrome +   
Multiple Self-healing Palmoplantar Carcinoma  
Myocardial Ischemia +   
neurogenic bowel 
Oculocerebrocutaneous Syndrome 
Omphalocele, Diaphragmatic Hernia, and Radial Ray Defects 
Ophthalmomandibulomelic Dysplasia 
osmotic diarrhea 
Pancytopenia and Occlusive Vascular Disease 
Parasitic Intestinal Diseases +   
Patternless Dermal Ridges 
Peripapillary Atrophy, Beta Type 
peripheral vascular disease +   
Persistent Hyperplastic Primary Vitreous, Autosomal Dominant 
Persistent Hyperplastic Primary Vitreous, Autosomal Recessive  
Peutz-Jeghers syndrome  
pigmented paravenous chorioretinal atrophy  
pneumatosis cystoides intestinalis 
poikiloderma with neutropenia  
Pontine Microangiopathy and Leukoencephalopathy, Autosomal Dominant  
Port-Wine Stain +   
postgastrectomy syndrome +  
primary congenital glaucoma +   
prolidase deficiency  
protein-losing enteropathy +   
pseudoxanthoma elasticum +   
Pulmonary Vein Stenosis 
pulmonary venoocclusive disease +   
Radial Drusen, Autosomal Dominant 
rectal disease +   
renal hypomagnesemia 5 with ocular involvement  
Reperfusion Injury +   
Retinal Aplasia 
Retinal Dysplasia +   
Retinal Dystrophy, Early Onset Severe  
retinal vascular disease +   
retinal vasculopathy with cerebral leukodystrophy  
retinitis pigmentosa +   
Retinohepatoendocrinologic Syndrome 
Rhegmatogenous Retinal Detachment, Autosomal Dominant  
Ridges-off-the-end Syndrome 
Rothmund-Thomson syndrome +   
Satoyoshi Syndrome 
scimitar syndrome +   
Sclerema Neonatorum 
secretory diarrhea +   
sitosterolemia +   
Skin/Hair/Eye Pigmentation, Variation In, 1  
Skin/Hair/Eye Pigmentation, Variation In, 10  
Skin/Hair/Eye Pigmentation, Variation In, 11  
Skin/Hair/Eye Pigmentation, Variation In, 4  
Skin/Hair/Eye Pigmentation, Variation In, 5  
Skin/Hair/Eye Pigmentation, Variation In, 6  
Skin/Hair/Eye Pigmentation, Variation In, 7  
Skin/Hair/Eye Pigmentation, Variation In, 8  
Skin/Hair/Eye Pigmentation, Variation In, 9  
Spinal Cord Vascular Diseases +   
splenic infarction 
Spondyloocular Syndrome, Autosomal Recessive  
Spontaneous Coronary Artery Dissection  
Steatorrhea +   
Stickler Syndrome, Type I, Nonsyndromic Ocular  
STING-associated vasculopathy with onset in infancy  
Superior Vena Cava Syndrome  
supine hypotensive syndrome 
telangiectasis +   
thoracic outlet syndrome +  
thrombosis +   
Trehalase Deficiency  
trichothiodystrophy +   
tropical sprue 
umbilical hernia +   
Urban Schosser Spohn Syndrome  
varicose veins +   
Vascular Fistula +   
vascular hemostatic disease +   
Vascular Hyalinosis 
Vascular Neoplasms 
Vascular System Injuries  
Vascular Tissue Neoplasms +   
vasculitis +   
vein disease +   
Veno-Occlusive Disease +   
venous insufficiency +   
vitelliform macular dystrophy +   
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia  
Walker-Warburg syndrome +   
Weill-Marchesani syndrome +   
Whipple disease +  
Winter Shortland Temple Syndrome  
X-Linked Macular Dystrophy +   
xeroderma pigmentosum +   
Zollinger-Ellison syndrome  

Primary IDs: MESH:C564750
Alternate IDs: OMIM:277175

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