Hyperpigmented/hypopigmented macules
Symptom Information:
Symptom ID: | HPO:0007441 | ||||
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) Generalized abnormality of skin(HPO:0011354) Abnormality of skin morphology(HPO:0011121) Abnormality of skin pigmentation(HPO:0001000) Hyperpigmentation of the skin(HPO:0000953) Mixed hypo- and hyperpigmentation of the skin(HPO:0009123) Hyperpigmented/hypopigmented macules(HPO:0007441) Hypopigmentation of the skin(HPO:0001010) Mixed hypo- and hyperpigmentation of the skin(HPO:0009123) Hyperpigmented/hypopigmented macules(HPO:0007441) Localized skin lesion(HPO:0011355) Hyperpigmented/hypopigmented macules(HPO:0007441) MedDRA: |
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Database Frequency: | 6 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Dyschromatosis symmetrica hereditaria | (Orphanet:41) |
Dyschromatosis universalis | (Orphanet:241) |
Dyschromatosis universalis hereditaria 1 | (OMIM:127500) |
Dyschromatosis universalis hereditaria 2 | (OMIM:612715) |
Dyschromatosis universalis hereditaris 3 | (OMIM:615402) |
Hypopigmentation-punctate palmoplantar keratoderma syndrome | (Orphanet:324561) |