MeSH Browser

MeSH Heading: Skin Diseases, Genetic
Tree Number(s): C16.320.850; C17.800.827
Unique ID: D012873
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D012873
Annotation: general or unspecified; prefer specifics
Scope Note: Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism.
Entry Version: SKIN DIS GENET
Entry Term(s): Genetic Skin Diseases
NLM Classification #: WR 218
Previous Indexing: Skin Diseases (1975-1997)
Public MeSH Note: 98
History Note: 98; use explode 1970-97
Date Established: 1998/01/01
Date of Entry: 1999/01/01
Revision Date: 2019/05/24

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Skin Diseases, Genetic MeSH Descriptor Data 2024