MeSH Browser

MeSH Heading: Optic Atrophies, Hereditary
Tree Number(s): C10.292.700.225.500; C10.574.500.662; C11.270.564; C11.640.451.451; C16.320.290.564; C16.320.400.630
Unique ID: D015418
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D015418
Scope Note: Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER).
Entry Term(s): Hereditary Optic Atrophy; Optic Atrophy, Hereditary
NLM Classification #: WW 280
Previous Indexing: Optic Atrophy/genetics (1966-1988)
Public MeSH Note: 2000; see OPTIC ATROPHY, HEREDITARY 1991-1999, see NEUROPATHIES, HEREDITARY MOTOR AND SENSORY 1989-1990
History Note: 2000(1989)
Date Established: 1991/01/01
Date of Entry: 1988/06/07
Revision Date: 2001/07/25

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)

Optic Atrophies, Hereditary MeSH Descriptor Data 2024