Generalized hyperpigmentation

Symptom Information:

Symptom ID: HPO:0007440
Synonyms:
Melanoderma [Orphanet:23530]
Melanoderma (disorder) [Orphanet:23530]
Generalized hyperpigmentation [OMIM:Generalized hyperpigmentation]
Diffuse/generalised skin hyperpigmentation/melanoderma [Orphanet:23530]
Melanodermia [Orphanet:23530]
Melanoderma [MedDRA:10027146]
Black spot [MedDRA:10027146]
Leucomelanoderma [MedDRA:10027146]
Melanodermia [MedDRA:10027146]
Leukomelanoderma [MedDRA:10027146]
Quality:
Cross references:
HPO:0000953 "Hyperpigmentation of the skin" [Orphanet:23530]
Orphanet:23530 "Diffuse/generalised skin hyperpigmentation/melanoderma" [Orphanet:23530]
OMIM: "Generalized hyperpigmentation" [OMIM:Generalized hyperpigmentation]
UMLS:C0221436 "Melanoderma" [Orphanet:23530]
Is a (Direct Parents):
MedDRA Hyperpigmentation disorders
HPO         Hyperpigmentation of the skin
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)
             Generalized abnormality of skin(HPO:0011354)
                Abnormality of skin morphology(HPO:0011121)
                   Abnormality of skin pigmentation(HPO:0001000)
                      Hyperpigmentation of the skin(HPO:0000953)
                         Generalized hyperpigmentation(HPO:0007440)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Pigmentation disorders(MedDRA:10035023)
       Hyperpigmentation disorders(MedDRA:10020713)
          Generalized hyperpigmentation(HPO:0007440)
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLYDEATH (OMIM:208910)
Acromelanosis (Orphanet:39)
Cushing disease (Orphanet:96253)
Gaucher disease type 1 (Orphanet:77259)
Hemochromatosis type 2 (Orphanet:79230)
Hemochromatosis type 3 (Orphanet:225123)
Hemochromatosis type 4 (Orphanet:139491)
Hemochromatosis, type 1 (OMIM:235200)
Hemochromatosis, type 2A (OMIM:602390)
Insulin-resistance syndrome type A (Orphanet:2297)
MELANOSIS, UNIVERSAL (OMIM:155800)