Generalized hyperpigmentation
Symptom Information:
Symptom ID: | HPO:0007440 | ||||||||||
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) Generalized hyperpigmentation(HPO:0007440) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Pigmentation disorders(MedDRA:10035023) Hyperpigmentation disorders(MedDRA:10020713) Generalized hyperpigmentation(HPO:0007440) |
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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) |