Hypopigmentation [hypopigmentace]
- Terms
-
hypomelanóza
snížená pigmentace
-
Hypomelanosis
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.
- Annotation
- do not confuse with HYPERPIGMENTATION
- DUI
- D017496 MeSH Browser
- CUI
- M0026547
- Previous indexing
- Pigmentation Disorders (1966-1992)
- History note
- 93
- Public note
- 93
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 3
- CO
- complications 1
- CN
- congenital
- DI
- diagnosis 3
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy 1
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology 3
- GE
- genetics
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 1
- PP
- physiopathology
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 2
- UR
- urine
- VE
- veterinary
- VI
- virology 1
Hernandez Fragoso syndrome Disease MeSH Browser
Leukonychia totalis Disease MeSH Browser
external ophthalmoplegia, synergistic divergence, jaw winking, and oculocutaneous hypopigmentation Disease MeSH Browser