Hyperpigmented/hypopigmented macules

Symptom Information:

Symptom ID: HPO:0007441
Synonyms:
Hyperpigmented/hypopigmented macules (dorsum hands and feet, face) [OMIM:Hyperpigmented/hypopigmented macules (dorsum hands and feet, face)]
Hyperpigmented/hypopigmented macules (trunk, extremities, occasionally face) [OMIM:Hyperpigmented/hypopigmented macules (trunk, extremities, occasionally face)]
Quality:
Cross references:
OMIM: "Hyperpigmented/hypopigmented macules (dorsum hands and feet, face)" [OMIM:Hyperpigmented/hypopigmented macules (dorsum hands and feet, face)]
OMIM: "Hyperpigmented/hypopigmented macules (trunk, extremities, occasionally face)" [OMIM:Hyperpigmented/hypopigmented macules (trunk, extremities, occasionally face)]
Is a (Direct Parents):
HPO         Localized skin lesion
HPO         Mixed hypo- and hyperpigmentation 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)
             Localized skin lesion(HPO:0011355)
                Hyperpigmented/hypopigmented macules(HPO:0007441)
             Generalized abnormality of skin(HPO:0011354)
                Abnormality of skin morphology(HPO:0011121)
                   Abnormality of skin pigmentation(HPO:0001000)
                      Hypopigmentation of the skin(HPO:0001010)
                         Mixed hypo- and hyperpigmentation of the skin(HPO:0009123)
                            Hyperpigmented/hypopigmented macules(HPO:0007441)
                      Hyperpigmentation of the skin(HPO:0000953)
                         Mixed hypo- and hyperpigmentation of the skin(HPO:0009123)
                            Hyperpigmented/hypopigmented macules(HPO:0007441)
MedDRA:
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)