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Term:
Skin/Hair/Eye Pigmentation, Variation In, 7 (DOID:9007207)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1)
Parent Terms Term With Siblings Child Terms
Skin Abnormalities +     
acanthosis nigricans +   
acrodermatitis +   
ADULT syndrome  
Anetoderma +   
Anonychia with Flexural Pigmentation 
Argyria 
AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS  
BADS syndrome 
Barber-Say syndrome  
Basaran Yilmaz Syndrome  
Beare-Stevenson cutis gyrata syndrome  
Blepharophimosis Syndrome Type 1  
Blepharophimosis Syndrome Type 2  
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 +   
Carney complex +   
cocoon syndrome  
conjunctival pigmentation 
Cutaneous Hemangiomatosis with Associated Features 
Dermal Ridges, Nelson Syndrome 
Dermal Ridges, Patternless 
Dermoodontodysplasia 
dyschromatosis symmetrica hereditaria  
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
Dyskeratosis, Hereditary Benign Intraepithelial 
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 
FLOTCH Syndrome 
Graying of Hair, Precocious 
Griscelli syndrome +   
Grouped Pigmentation of the Macula 
Hairy Palms and Soles 
Heterochromia Iridis  
Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated with Cerebral Capillary Malformations  
Hyperpigmentation +   
Hypohidrosis with Abnormal Palmar Dermal Ridges 
Hypopigmentation +   
hypopigmentation of eyelid 
ichthyosis +   
Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 
Infantile Cataract, Skin Abnormalities, Glutamate Excess, and Impaired Intellectual Development  
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
lethal restrictive dermopathy  
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2  
LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3  
Macules Hereditary Congenital Hypopigmented and Hyperpigmented 
Michelin Tire Baby Syndrome +   
Microphthalmia, Syndromic 7  
multiple pterygium syndrome +   
neonatal jaundice +   
Oculocerebral Hypopigmentation Syndrome Type Preus 
Oculocerebrocutaneous Syndrome 
PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING  
Pigmented Purpuric Eruption 
poikiloderma with neutropenia  
Poikiloderma, Hereditary Sclerosing +   
Port-Wine Stain +   
Prolidase Deficiency  
pseudoxanthoma elasticum +   
Pterygium Colli, Isolated 
Red Skin Pigment Anomaly of New Guinea 
Reticulate Pigmentary Disorder, with Systemic Manifestations  
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 and Pigmentary Defects  
Thumb Deformity, Alopecia, Pigmentation Anomaly 
Trichothiodystrophy Syndromes +   
Urban Schosser Spohn Syndrome 
urticaria pigmentosa  
Vascular Hyalinosis 
Waardenburg Syndrome Type 4 +   
White Forelock with Malformations 
Whyte Murphy Syndrome 
Winter Shortland Temple Syndrome  
xeroderma pigmentosum +   
yellow nail syndrome +  

Synonyms
Exact Synonyms: Shep7 ;   Skin-Hair-Eye Pigmentation 7, Blond-Brown Hair ;   Skin-Hair-Eye Pigmentation 7, Dark-Light Skin
Primary IDs: MESH:C567155 ;   RDO:0015305

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