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Diseases

Hyperpigmentation

hyperpigmentation

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Hyperpigmentation
Standard Disease Name
hyperpigmentation
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D017495
OMIM ID
MTHU001136|MTHU016089|MTHU016138
UMLS ID
C0162834
HPO ID
No data

Description and Extensions

Description
NCI2016_NICHD_1602D:Abnormal darkening of the skin.|NCI2016_CTCAE_1602D:A disorder characterized by darkening of the skin due to excessive melanin deposition.|NCI2016_02D:Darkening of the skin due to excessive melanin deposition. Causes include skin injuries, pregnancy, eczema, and Addison disease.|MSH2017_2016_08_12:Excessive pigmentation of the skin, usually as a result of increased epidermal or dermal melanin pigmentation, hypermelanosis. Hyperpigmentation can be localized or generalized. The condition may arise from exposure to light, chemicals or other substances, or from a primary metabolic imbalance.|HPO2016_07_04:A darkening of the skin related to an increase in melanin production and deposition. [HPO:probinson]|CHV2011_02:the increase in the natural color of the skin|CHV2011_02:the increase in the natural color of the skin|CHV2011_02:the increase in the natural color of the skin|CHV2011_02:the increase in the natural color of the skin
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
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BRAF
B-Raf proto-oncogene, serine/threonine kinase
B-Raf proto-oncogene, serine/threonine kinase
03
KCNMA1
potassium calcium-activated channel subfamily M alpha 1
potassium calcium-activated channel subfamily M alpha 1