Descriptor English: | Hypopigmentation | ||||
Descriptor Spanish: |
Hipopigmentación
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Descriptor Portuguese: | Hipopigmentação | ||||
Descriptor French: | Hypopigmentation | ||||
Entry term(s): |
Hypomelanoses Hypomelanosis |
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Tree number(s): |
C17.800.621.440 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D017496 | ||||
Scope note: | A condition caused by a deficiency or a loss of melanin pigmentation in the epidermis, also known as hypomelanosis. Hypopigmentation can be localized or generalized, and may result from genetic defects, trauma, inflammation, or infections. |
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Annotation: | do not confuse with HYPERPIGMENTATION |
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Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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Previous Indexing: |
Pigmentation Disorders (1966-1992) |
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Public MeSH Note: | 93 |
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History Note: | 93 |
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DeCS ID: | 30691 | ||||
Unique ID: | D017496 | ||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
Date Established: | 1993/01/01 | ||||
Date of Entry: | 1992/05/20 | ||||
Revision Date: | 2016/07/01 |
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Hypopigmentation
- Preferred
Concept UI |
M0026547 |
Scope note | A condition caused by a deficiency or a loss of melanin pigmentation in the epidermis, also known as hypomelanosis. Hypopigmentation can be localized or generalized, and may result from genetic defects, trauma, inflammation, or infections. |
Preferred term | Hypopigmentation |
Entry term(s) |
Hypomelanoses Hypomelanosis |
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