Partial albinism

Symptom Information:

Symptom ID: HPO:0007443
Synonyms:
Congenital partial albinism (leucoderma) on face, trunk, or limbs [HPO:0007443]
Congenital partial albinism on face, trunk, or limbs [HPO:0007443]
Congenital partial albinism (leukoderma) on face, trunk, or limbs [OMIM:Congenital partial albinism (leukoderma) on face, trunk, or limbs]
Quality:
Cross references:
OMIM: "Congenital partial albinism (leukoderma) on face, trunk, or limbs" [OMIM:Congenital partial albinism (leukoderma) on face, trunk, or limbs]
Is a (Direct Parents):
HPO         Hypopigmentation of the skin
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)
                         Partial albinism(HPO:0007443)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Albinism-deafness syndrome (Orphanet:998)
Oculocutaneous albinism type 3 (Orphanet:79433)
Piebaldism (Orphanet:2884)
WAARDENBURG SYNDROME, TYPE 2A (OMIM:193510)
Waardenburg syndrome (Orphanet:3440)
Waardenburg syndrome type 1 (Orphanet:894)
Waardenburg syndrome type 2 (Orphanet:895)
Waardenburg syndrome type 3 (Orphanet:896)