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Ontology Browser

Skin/Hair/Eye Pigmentation, Variation In, 7 (DOID:9007207)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Skin Abnormalities +     
acanthosis nigricans +   
acrodermatitis +   
ADULT syndrome  
Anetoderma +   
Anonychia with Flexural Pigmentation 
Autoinflammation with Arthritis and Dyskeratosis  
BADS syndrome 
Barber-Say syndrome  
Basaran Yilmaz Syndrome  
Beare-Stevenson cutis gyrata syndrome  
Blepharophimosis with Ptosis, Syndactyly, and Short Stature 
blepharophimosis, ptosis, and epicanthus inversus syndrome +   
Bloch-Sulzberger syndrome +   
Book Syndrome 
Bullous Dystrophy, Hereditary Macular Type 
C1q Deficiency  
Cafe-au-Lait Spots +   
Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma  
Carney complex +   
conjunctival pigmentation 
Cutaneous Hemangiomatosis with Associated Features 
Dermal Ridges, Nelson Syndrome 
dyschromatosis symmetrica hereditaria  
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
ectodermal dysplasia +   
Ehlers-Danlos syndrome +   
Elejalde Disease 
epidermolysis bullosa +   
Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract 
Erosive Arthropathy 
Familial Dyskeratotic Comedones 
Familial Popliteal Pterygium Syndrome 
fetal encasement syndrome  
FLOTCH Syndrome 
Griscelli syndrome +   
Grouped Pigmentation of the Macula 
Hairy Palms and Soles 
Hereditary Benign Intraepithelial Dyskeratosis 
Hereditary Sclerosing Poikiloderma +   
Heterochromia Iridis  
Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated with Cerebral Capillary Malformations  
Hyperpigmentation +   
Hypohidrosis with Abnormal Palmar Dermal Ridges 
Hypopigmentation +   
ichthyosis +   
Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 
Infantile Cataract, Skin Abnormalities, Glutamate Excess, and Impaired Intellectual Development  
Isolated Pterygium Colli 
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
lethal restrictive dermopathy  
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Macules Hereditary Congenital Hypopigmented and Hyperpigmented 
MLS syndrome +   
multiple benign circumferential skin creases on limbs +   
multiple pterygium syndrome +   
Multiple Self-healing Palmoplantar Carcinoma  
neonatal jaundice +   
Oculocerebral Hypopigmentation Syndrome Type Preus 
Oculocerebrocutaneous Syndrome 
Patternless Dermal Ridges 
Pigmented Purpuric Eruption 
poikiloderma with neutropenia  
Port-Wine Stain +   
Precocious Graying of Hair 
prolidase deficiency  
pseudoxanthoma elasticum +   
Red Skin Pigment Anomaly of New Guinea 
Ridges-off-the-end Syndrome 
Rothmund-Thomson syndrome +   
Russell-Silver Syndrome, X-Linked 
Sclerema Neonatorum 
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  
stromal corneal pigmentation 
Symmetric Acroleukopathy  
Tang Hsi Ryu Syndrome 
terminal osseous dysplasia  
Thumb Deformity, Alopecia, Pigmentation Anomaly 
trichothiodystrophy +   
Urban Schosser Spohn Syndrome  
urticaria pigmentosa  
Vascular Hyalinosis 
Waardenburg Syndrome Type 4 +   
White Forelock with Malformations 
Whyte Murphy Syndrome 
Winter Shortland Temple Syndrome  
X-linked reticulate pigmentary disorder  
xeroderma pigmentosum +   
yellow nail syndrome +  

Exact Synonyms: Shep7 ;   Skin-Hair-Eye Pigmentation 7, Blond-Brown Hair ;   Skin-Hair-Eye Pigmentation 7, Dark-Light Skin
Primary IDs: MESH:C567155

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