Spotty hypopigmentation

Symptom Information:

Symptom ID: HPO:0005590
Synonyms:
Patchy hypopigmentation [HPO:0005590]
Hypopigmented skin patch [Orphanet:23520]
Patchy hypopigmentation [OMIM:Patchy hypopigmentation]
Spotty hypopigmentation [OMIM:Spotty hypopigmentation]
Irregular/patchy skin hypopigmentation [Orphanet:23520]
Quality:
Cross references:
HPO:0001053 "Hypopigmented skin patches" [Orphanet:23520]
Orphanet:23520 "Irregular/patchy skin hypopigmentation" [Orphanet:23520]
OMIM: "Patchy hypopigmentation" [OMIM:Patchy hypopigmentation]
OMIM: "Spotty hypopigmentation" [OMIM:Spotty hypopigmentation]
Is a (Direct Parents):
HPO         Hypopigmented skin patches
Orphanet 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)
             Localized skin lesion(HPO:0011355)
                Hypopigmented skin patches(HPO:0001053)
                   Spotty hypopigmentation(HPO:0005590)
             Generalized abnormality of skin(HPO:0011354)
                Abnormality of skin morphology(HPO:0011121)
                   Abnormality of skin pigmentation(HPO:0001000)
                      Hypopigmentation of the skin(HPO:0001010)
                         Hypopigmented skin patches(HPO:0001053)
                            Spotty hypopigmentation(HPO:0005590)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Acromelanosis (Orphanet:39)
Bloom syndrome (Orphanet:125)
Dyschromatosis symmetrica hereditaria (Orphanet:41)
Dyschromatosis universalis hereditaria 1 (OMIM:127500)
Dyschromatosis universalis hereditaria 2 (OMIM:612715)
Dyschromatosis universalis hereditaris 3 (OMIM:615402)
Hereditary acrokeratotic poikiloderma of Kindler-Weary (Orphanet:306539)
Intellectual deficit, X-linked, Nascimento type (Orphanet:163956)
MELAS (Orphanet:550)
SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES (OMIM:615789)