Descriptor English: | Distal Myopathies | ||||||
Descriptor Spanish: |
Miopatías Distales
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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 |
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Tree number(s): |
C05.651.534.500.074 C10.668.491.175.500.074 C16.320.577.074 |
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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. |
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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 VI virology |
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Previous Indexing: |
Muscular Diseases (1965-2004) Muscular Dystrophies (1966-2004) |
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Public MeSH Note: | 2005; see MUSCULAR DYSTROPHIES 2000-2004 |
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History Note: | 2005; use MUSCULAR DYSTROPHIES 2000-2004 |
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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 |
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Distal Myopathies
- Preferred
Tibial Muscular Dystrophy
- Narrower
Welander Distal Myopathy
- Narrower
Tibial Muscular Dystrophy, Tardive
- Narrower
Distal Myopathy 1
- Narrower
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 |
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 |
Concept UI |
M0464101 |
Preferred term | Welander Distal Myopathy |
Entry term(s) |
Distal Myopathy, Welander Myopathy, Distal, Swedish |
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 |
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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