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:
TMD
Finnish tibial muscular dystrophy
Distal titinopathy
Distal myopathy, Udd type
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))
- OMIM:600334 (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). - Attributed (The ICD code is attributed by Orphanet).)
- UMLS:C1838244 (E (Exact mapping: the two concepts are equivalent))
definition citation
- Orphanet
expertlink
- https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=609
hasDbXref
- MeSH:C536815
- OMIM:600334
- UMLS:C1450052
- UMLS:C1838244
- ICD-10:G71.0
has age of onset
- http://www.orpha.net/ORDO/Orphanet_409948
has inheritance
- http://www.orpha.net/ORDO/Orphanet_409930
- http://www.orpha.net/ORDO/Orphanet_409929
has point prevalence average value
- 20.0
- 6.0
has point prevalence range
- http://www.orpha.net/ORDO/Orphanet_409975
- http://www.orpha.net/ORDO/Orphanet_409977
notation
- ORPHA:609
part of
- http://www.orpha.net/ORDO/Orphanet_209053
- http://www.orpha.net/ORDO/Orphanet_206650
present in
- http://www.orpha.net/ORDO/Orphanet_409984
- http://www.orpha.net/ORDO/Orphanet_410065
Term relations
Subclass of:
Related from: