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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Albinism +   
alopecia areata +   
Cole Disease  
dermatitis herpetiformis +   
ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES  
epidermolysis bullosa acquisita 
External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation 
Hernandez Fragoso Syndrome 
hypomelanosis of Ito  
hypopigmentation of eyelid 
HYPOPIGMENTATION, ORGANOMEGALY, AND DELAYED MYELINATION AND DEVELOPMENT  
Leukonychia Totalis +   
Obesity and Hypopigmentation  
pemphigoid +   
pemphigus +   
psoriasis +   
psoriatic arthritis  
Raindrop Hypopigmentation 
vitiligo +   
An autoimmune disease that causes depigmentation of patches of skin resulting from loss of function or death of melanoctyes. (DO)
Vogt-Koyanagi-Harada disease  
Yemenite Deaf-Blind Hypopigmentation Syndrome 

Synonyms
Exact Synonyms: SLEV1 ;   VTLG ;   vitiligo-related systemic lupus erythematosus
Related Synonyms: AIS1 ;   AIS2 ;   AIS3 ;   AIS4 ;   AUTOIMMUNE DISEASE SUSCEPTIBILITY LOCUS, CHROMOSOME 1p-RELATED ;   AUTOIMMUNE DISEASE SUSCEPTIBILITY LOCUS, CHROMOSOME 4-RELATED ;   AUTOIMMUNE DISEASE SUSCEPTIBILITY LOCUS, CHROMOSOME 7-RELATED ;   AUTOIMMUNE DISEASE SUSCEPTIBILITY LOCUS, CHROMOSOME 8-RELATED ;   Autoimmune Disease, Susceptibility To, 1 ;   Autoimmune Disease, Susceptibility To, 2
Primary IDs: MESH:D014820
Alternate IDs: MIM:193200 ;   MIM:606579 ;   MIM:607836 ;   MIM:608391 ;   MIM:608392 ;   MIM:609400
Xrefs: EFO:0004208 ;   GARD:10751 ;   ICD10CM:L80 ;   ICD9CM:709.01 ;   NCI:C26915
Definition Sources: http://en.wikipedia.org/wiki/Vitiligo "DO" "DO"

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