Vitiligo

Symptom Information:

Symptom ID: HPO:0001045
Synonyms:
Vitiligo [OMIM:Vitiligo]
Vitiligo (1 patient) [OMIM:Vitiligo (1 patient)]
Vitiligo [MedDRA:10047642]
Quality:
Cross references:
OMIM: "Vitiligo" [OMIM:Vitiligo]
OMIM: "Vitiligo (1 patient)" [OMIM:Vitiligo (1 patient)]
UMLS:C0042900 "Vitiligo" [HPO:0001045]
Is a (Direct Parents):
MedDRA Skin autoimmune disorders NEC
HPO         Abnormality of skin pigmentation
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Abnormality of skin morphology(HPO:0011121)
                   Abnormality of skin pigmentation(HPO:0001000)
                      Vitiligo(HPO:0001045)
MedDRA:
Immune system disorders(MedDRA:10021428)
    Autoimmunity(HPO:0002960)
       Skin autoimmune disorders NEC(MedDRA:10052738)
          Vitiligo(HPO:0001045)
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
Autosomal recessive spastic paraplegia type 23 (Orphanet:101003)
Deafness - vitiligo - achalasia (Orphanet:3239)
Ermine phenotype (Orphanet:999)
FANCONI ANEMIA, COMPLEMENTATION GROUP P (OMIM:613951)
Familial progressive hyperpigmentation (Orphanet:79146)
MELAS (Orphanet:550)
PLCG2-associated antibody deficiency and immune dysregulation (Orphanet:300359)
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION (OMIM:607944)
Stiff person syndrome (Orphanet:3198)
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (OMIM:606579)
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 (OMIM:193200)
Vitiligo-associated autoimmune disease (Orphanet:247871)