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Descriptor English: Distal Myopathies
Descriptor Spanish: Miopatías Distales
Descriptor miopatías distales
Entry term(s) distrofia muscular distal
Scope note: Grupo heterogéneo de trastornos genéticos caracterizados por ATROFIA MUSCULAR y DEBILIDAD MUSCULAR progresivas que comienzan en manos, piernas o pies. La mayoría son formas autosómicas dominantes que comienzan en la edad adulta. Otras son autosómicas recesivas.Grupo heterogéneo de trastornos genéticos caracterizados por ATROFIA MUSCULAR y DEBILIDAD MUSCULAR progresivas que comienzan en las manos, piernas o pies. La mayoría son formas autosómicas dominantes de comienzo en la edad adulta. Otras son autosómicas recesivas.
Descriptor Portuguese: Miopatias Distais
Descriptor French: Myopathies distales
Entry term(s): Distal 1 Myopathies
Distal 1 Myopathy
Distal Muscular Dystrophies
Distal Muscular Dystrophy
Distal Myopathy
Distal Myopathy 1
Distal Myopathy 1s
Distal Myopathy Markesbery Griggs Type
Distal Myopathy Markesbery-Griggs Type
Distal Myopathy, Laing
Distal Myopathy, Udd
Distal Myopathy, Welander
Finnish Markesbery Muscular Dystrophy
Finnish-Markesbery Muscular Dystrophy
Laing Distal Myopathy
Laing Early Onset Distal Myopathy
Laing Early-Onset Distal Myopathy
Muscular Dystrophies, Distal
Muscular Dystrophies, Tibial
Muscular Dystrophy, Distal
Muscular Dystrophy, Distal, Late-Onset, Autosomal Dominant
Muscular Dystrophy, Finnish-Markesbery
Muscular Dystrophy, Tibial
Muscular Dystrophy, Udd-Markesbery
Myopathies, Distal
Myopathies, Distal 1
Myopathy 1, Distal
Myopathy 1s, Distal
Myopathy, Distal
Myopathy, Distal 1
Myopathy, Distal, Early-Onset, Autosomal Dominant
Myopathy, Distal, Swedish
Myopathy, Laing Distal
Myopathy, Late Distal Hereditary
Myopathy, Udd
Myopathy, Udd Distal
Tardive Tibial Muscular Dystrophy
Tibial Muscular Dystrophy
Tibial Muscular Dystrophy, Tardive
Udd Distal Myopathy
Udd Markesbery Muscular Dystrophy
Udd Myopathy
Udd-Markesbery Muscular Dystrophy
Welander Distal Myopathy
Tree number(s): C05.651.534.500.074
C10.668.491.175.500.074
C16.320.577.074
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D049310
Scope note: A heterogeneous group of genetic disorders characterized by progressive MUSCULAR ATROPHY and MUSCLE WEAKNESS beginning in the hands, the legs, or the feet. Most are adult-onset autosomal dominant forms. Others are autosomal recessive.
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
VI virology
Previous Indexing: Muscular Diseases (1965-2004)
Muscular Dystrophies (1966-2004)
Public MeSH Note: 2005; see MUSCULAR DYSTROPHIES 2000-2004
History Note: 2005; use MUSCULAR DYSTROPHIES 2000-2004
DeCS ID: 38612
Unique ID: D049310
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2005/01/01
Date of Entry: 2004/07/07
Revision Date: 2018/10/10
Distal Myopathies - Preferred
Concept UI M0335585
Scope note A heterogeneous group of genetic disorders characterized by progressive MUSCULAR ATROPHY and MUSCLE WEAKNESS beginning in the hands, the legs, or the feet. Most are adult-onset autosomal dominant forms. Others are autosomal recessive.
Preferred term Distal Myopathies
Entry term(s) Distal Muscular Dystrophies
Distal Muscular Dystrophy
Distal Myopathy
Muscular Dystrophies, Distal
Muscular Dystrophy, Distal
Myopathies, Distal
Myopathy, Distal
Tibial Muscular Dystrophy - Narrower
Concept UI M0464105
Preferred term Tibial Muscular Dystrophy
Entry term(s) Distal Myopathy, Udd
Finnish Markesbery Muscular Dystrophy
Finnish-Markesbery Muscular Dystrophy
Muscular Dystrophies, Tibial
Muscular Dystrophy, Finnish-Markesbery
Muscular Dystrophy, Tibial
Muscular Dystrophy, Udd-Markesbery
Myopathy, Udd
Myopathy, Udd Distal
Udd Distal Myopathy
Udd Markesbery Muscular Dystrophy
Udd Myopathy
Udd-Markesbery Muscular Dystrophy
Welander Distal Myopathy - Narrower
Concept UI M0464101
Preferred term Welander Distal Myopathy
Entry term(s) Distal Myopathy, Welander
Myopathy, Distal, Swedish
Tibial Muscular Dystrophy, Tardive - Narrower
Concept UI M0531276
Preferred term Tibial Muscular Dystrophy, Tardive
Entry term(s) Distal Myopathy Markesbery Griggs Type
Distal Myopathy Markesbery-Griggs Type
Tardive Tibial Muscular Dystrophy
Distal Myopathy 1 - Narrower
Concept UI M000644437
Preferred term Distal Myopathy 1
Entry term(s) Distal 1 Myopathies
Distal 1 Myopathy
Distal Myopathy 1s
Distal Myopathy, Laing
Laing Distal Myopathy
Laing Early Onset Distal Myopathy
Laing Early-Onset Distal Myopathy
Muscular Dystrophy, Distal, Late-Onset, Autosomal Dominant
Myopathies, Distal 1
Myopathy 1, Distal
Myopathy 1s, Distal
Myopathy, Distal 1
Myopathy, Distal, Early-Onset, Autosomal Dominant
Myopathy, Laing Distal
Myopathy, Late Distal Hereditary



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