Piebaldism

Symptom Information:

Symptom ID: HPO:0007544
Synonyms:
Partial albinism (disorder) [Orphanet:24360]
Piebaldism [Orphanet:24360]
Piebaldism [OMIM:Piebaldism]
White forelock/piebaldism [Orphanet:24360]
Quality:
Cross references:
Orphanet:24360 "White forelock/piebaldism" [Orphanet:24360]
OMIM: "Piebaldism" [OMIM:Piebaldism]
UMLS:C0080024 "Piebaldism" [Orphanet:24360]
Is a (Direct Parents):
HPO         Hypopigmentation of the skin
Orphanet Abnormality of the hair
Orphanet White forelock
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)
                      Hypopigmentation of the skin(HPO:0001010)
                         Piebaldism(HPO:0007544)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Albinism-deafness syndrome (Orphanet:998)
Piebaldism (Orphanet:2884)
Werner syndrome (Orphanet:902)