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
This is just here as a test because I lose it
Term information
database cross reference
- UMLS:C1450052 (E (Exact mapping: the two concepts are equivalent))
- ICD-10:G71.0 (Attributed (The ICD10 code is attributed by Orphanet))
- OMIM:600334 (E (Exact mapping: the two concepts are equivalent))
- UMLS:C1838244 (E (Exact mapping: the two concepts are equivalent))
- MeSH:C536815 (E (Exact mapping: the two concepts are equivalent))
- ICD-10:G71.0 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
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: