Spotty hypopigmentation
Symptom Information:
Symptom ID: | HPO:0005590 | |||||
Synonyms: |
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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) 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: |
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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) |