Tibial muscular dystrophy
http://www.orpha.net/ORDO/Orphanet_609
Tibial muscular dystrophy (TMD) is a distal myopathy characterized by weakness of the muscles of the anterior compartment of lower limbs, appearing in the fourth to seventh decade of life.
Synonyms: Distal myopathy, Udd type, Finnish tibial muscular dystrophy, TMD, Distal titinopathy, Udd myopathy
Term info
database cross reference
- ICD-10:G71.0 (NTBT (narrower term maps to a broader term))
- OMIM:600334 (E (exact mapping (the terms and the concepts are equivalent)))
- ICD-10:G71.0 (Attributed)
- MeSH:C536815 (E (exact mapping (the terms and the concepts are equivalent)))
- UMLS:C1838244 (E (exact mapping (the terms and the concepts are equivalent)))
- UMLS:C1450052 (E (exact mapping (the terms and the concepts are equivalent)))
definition citation
orphanet
hasDbXref
UMLS:C1838244, UMLS:C1450052, OMIM:600334, ICD-10:G71.0, MeSH:C536815
notation
ORPHA:609
Term relations
Subclass of:
- disease
- has_inheritance some autosomal recessive
- present_in some Finland and has_point_prevalence_range some 1-5 / 10 000 and has_point_prevalence_average_value value 20.0
- has_inheritance some autosomal dominant
- present_in some Europe and has_point_prevalence_range some 1-9 / 100 000 and has_point_prevalence_average_value value 6.0
- has_age_of_onset some adult
- part_of some Autosomal dominant distal myopathy
- part_of some Qualitative or quantitative defects of titin
Related from: