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Metadata
ID DOID:0111078
Name tibial muscular dystrophy
Definition A distal myopathy that is characterized by autosomal dominant inheritance of late-onset muscular dystrophy beginning in the anterior compartment of the legs that has_material_basis_in heterozygous mutation in the gene encoding the giant skeletal muscle protein titin (TTN) on chromosome 2q31.
https://www.ncbi.nlm.nih.gov/pubmed/12145747, https://www.ncbi.nlm.nih.gov/pubmed/196233, https://www.ncbi.nlm.nih.gov/pubmed/8503797
Xrefs

MESH:D049310

MIM:600334

ORDO:609

SNOMEDCT_US_2023_03_01:698846009

UMLS_CUI:C1838244

Subsets

DO_rare_slim

Synonyms

distal titinopathy [EXACT]

Finnish tibial muscular dystrophy [EXACT]

Tardive tibial muscular dystrophy [EXACT]

TMD [EXACT]

Udd myopathy [EXACT]

Udd type distal myopathy [EXACT]

Parent Relationships

is_a distal myopathy

is_a bone disease

is_a autosomal dominant disease

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