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Ontology Browser

Parent Terms Term With Siblings Child Terms
keratosis +     
Skin Abnormalities +     
skin disease +     
Achenbach syndrome 
Acneiform Eruptions +   
acquired hyperkeratosis 
acrodermatitis +   
acrokeratosis verruciformis  
actinic keratosis +   
allergic cutaneous vasculitis +   
Amniotic Band Syndrome +  
ancylostomiasis +  
Anetoderma +   
angioedema +   
asphyxia neonatorum +   
autoimmune disease of skin and connective tissue +   
Autoinflammation with Arthritis and Dyskeratosis  
Barber-Say syndrome  
Beare-Stevenson cutis gyrata syndrome  
benign neonatal seizures +   
Birt-Hogg-Dube syndrome  
Birth Injuries +   
Blepharophimosis with Ptosis, Syndactyly, and Short Stature 
blepharophimosis, ptosis, and epicanthus inversus syndrome +   
Bloch-Sulzberger syndrome +   
Book Syndrome 
Boudhina Yedes Khiari syndrome 
breast disease +   
C syndrome  
C1q Deficiency  
Caffey disease +   
Callosities +  
Carney complex +   
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal  
cercarial dermatitis 
chancroid +  
cholesteatoma +   
chronic ulcer of skin +   
Congenital Hyperinsulinism +   
congenital nystagmus +   
congenital syphilis +  
congenital toxoplasmosis 
contagious pustular dermatitis 
Curly Hair-Acral Keratoderma-Caries Syndrome 
Cutaneous Fistula 
Cutaneous Hemangiomatosis with Associated Features 
cutaneous lupus erythematosus +   
cutis laxa +   
Cutis Laxa-Marfanoid Syndrome 
cystic fibrosis +   
Dermal Fibrosis  
Dermal Ridges, Nelson Syndrome 
dermatitis +   
dermatomyositis +   
Duplication of Eyebrows with Stretchable Skin and Syndactyly 
dyskeratosis congenita +   
ectodermal dysplasia +   
Ectodermal Dysplasia-Skin Fragility Syndrome  
Eczematous Skin Diseases +   
Ehlers-Danlos syndrome +   
Elastosis Perforans Serpiginosa 
Elliott Ludman Teebi Syndrome 
endometriosis in scar of skin 
epidermal nevus +   
epidermolysis bullosa +   
Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract 
Erosive Arthropathy 
Erythema +   
erythematosquamous dermatosis 
erythrokeratodermia variabilis +   
exanthem +   
eyelid disease +   
FACES Syndrome 
facial dermatosis +   
Facial Ectodermal Dysplasia  
Familial Dyskeratotic Comedones 
Familial Popliteal Pterygium Syndrome 
fetal encasement syndrome  
fetal erythroblastosis +   
filariasis +   
Flynn Aird Syndrome 
Foot Diseases +   
Frank-Ter Haar syndrome  
Genetic Skin Diseases +   
granulomatosis with polyangiitis +   
hair disease +   
Hairy Palms and Soles 
hand dermatosis +  
hemorrhoid +   
Hereditary Benign Intraepithelial Dyskeratosis 
hereditary papulotranslucent acrokeratoderma 
Hereditary Sclerosing Poikiloderma +   
Hernandez Fragoso Syndrome 
hydrophthalmos +   
Hyperglycinemia, Transient Neonatal 
Hyperkeratosis Lenticularis Perstans 
Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated with Cerebral Capillary Malformations  
Hyperparathyroidism, Neonatal Severe Primary  
Hypohidrosis with Abnormal Palmar Dermal Ridges 
ichthyosis +   
Any of several generalized skin disorders characterized by dryness, roughness, and scaliness, due to hypertrophy of the stratum corneum epidermis. Most are genetic, but some are acquired, developing in association with other systemic disease or genetic syndrome.
Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 
Infantile Cataract, Skin Abnormalities, Glutamate Excess, and Impaired Intellectual Development  
Infantile Hypercalcemia +   
Infectious Skin Diseases +   
Isolated Pterygium Colli 
Johnston Aarons Schelley Syndrome 
juvenile xanthogranuloma 
Keratolytic Winter Erythema  
keratosis +   
keratosis follicularis +   
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
Kimura disease 
leg dermatosis 
lethal restrictive dermopathy  
lipomatosis +   
localized scleroderma +   
Macroepiphyseal Dysplasia, McAlister Coe Type 
MASS Syndrome  
mastocytosis +   
meconium aspiration syndrome  
Meconium Ileus  
Median Cleft Lip, Corpus Callosum, Lipoma, and Skin Polyps 
Mental Retardation, Joint Hypermobility, and Skin Laxity, with or without Metabolic Abnormalities 
Metabolic Skin Diseases +   
MLS syndrome +   
Mobius syndrome +   
mongolian spot 
Morgellons Disease 
multicentric reticulohistiocytosis 
multiple benign circumferential skin creases on limbs +   
multiple cutaneous and mucosal venous malformations  
Multiple Eruptive Milia 
multiple pterygium syndrome +   
Multiple Self-healing Palmoplantar Carcinoma  
nail disease +   
necrobiosis lipoidica 
Necrobiotic Disorders +  
Necrolytic Migratory Erythema 
neonatal abstinence syndrome 
Neonatal Alloimmune Thrombocytopenia  
neonatal anemia +   
neonatal diabetes +   
Neonatal Hyperbilirubinemia +   
Neonatal Hypoglycemia, Simulating Foetopathia Diabetica  
Neonatal Inflammatory Skin and Bowel Disease +   
Neonatal Pulmonary Hypertension  
Neonatal Sepsis  
Nephrogenic Fibrosing Dermopathy  
noninfectious dermatoses of eyelid +  
Oculocerebrocutaneous Syndrome 
ophthalmia neonatorum 
palmoplantar keratosis +   
Papulosquamous Skin Diseases +   
Patternless Dermal Ridges 
persistent fetal circulation syndrome  
phaeohyphomycosis +  
photosensitivity disease +   
pigmentation disease +   
poikiloderma with neutropenia  
porokeratosis +   
Port-Wine Stain +   
Posttransfusion Purpura  
Premature Infant Diseases +   
prolidase deficiency  
Pruritus +   
Pseudoatrophoderma Colli 
Pseudopyogenic Granuloma 
pseudoxanthoma elasticum +   
reactive cutaneous fibrous lesion +  
Ridges-off-the-end Syndrome 
rosacea +   
Rothmund-Thomson syndrome +   
Roy Maroteaux Kremp Syndrome 
scalp dermatosis +   
Sclerema Neonatorum 
sebaceous gland disease +   
seborrheic keratosis +   
severe combined immunodeficiency +   
Skin Abnormalities +   
skin atrophy 
Skin Neoplasms +   
skin sarcoidosis 
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  
sweat gland disease +   
thanatophoric dysplasia +   
transient neonatal thrombocytopenia 
Trichostasis Spinulosa 
trichothiodystrophy +   
tyrosinemia type II  
umbilical hernia +   
Upton Young Syndrome 
Urban Schosser Spohn Syndrome  
urticaria +   
Vascular Hyalinosis 
vascular skin disease +   
verruciform xanthoma of skin 
vitamin K deficiency bleeding  
Winter Shortland Temple Syndrome  
Wolman disease +   
xeroderma pigmentosum +   
 IFAP Syndrome +   

Exact Synonyms: Ichthyoses ;   Xeroderma ;   Xerodermas ;   non-syndromic ichthyosis
Narrow Synonyms: Ichthyosis, ASPRV1-related
Primary IDs: MESH:D007057 ;   RDO:0001008
Alternate IDs: OMIA:002099
Xrefs: NCI:C84776 ;   ORDO:79354
Definition Sources: "DO", "DO", "DO", "DO", MESH:D007057

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