Vitiligo
Symptom Information:
Symptom ID: | HPO:0001045 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |