Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

Ontology Browser
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) Pig: (1) Naked Mole-rat: (1) Green Monkey: (1)
Parent Terms Term With Siblings Child Terms
pigmentation disease +     
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 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 
contractures, pterygia, and spondylocarpotarsal fusion syndrome +   
Cutaneous Hemangiomatosis with Associated Features 
Dermal Ridges, Nelson Syndrome 
Dermoodontodysplasia 
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  
inflammatory poikiloderma with hair abnormalities and acral keratoses  
Isolated Pterygium Colli 
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Macules Hereditary Congenital Hypopigmented and Hyperpigmented 
MLS syndrome +   
multiple benign circumferential skin creases on limbs +   
Multiple Self-healing Palmoplantar Carcinoma  
neonatal jaundice +   
Neurodevelopmental Disorder with Hypotonia, Dysmorphic Facies, and Skin Abnormalities  
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 
restrictive dermopathy +   
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, 2  
Skin/Hair/Eye Pigmentation, Variation In, 3  
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  
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 +  

Synonyms
Exact Synonyms: SHEP7 ;   Skin-Hair-Eye Pigmentation 7, Blond-Brown Hair ;   Skin-Hair-Eye Pigmentation 7, Dark-Light Skin
Primary IDs: MESH:C567155
Alternate IDs: OMIM:611664

paths to the root