has material basis in germline mutation in TCAP autosomal recessive limb-girdle muscular dystrophy type 2G https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/autosomal_recessive_limb_girdle_muscular_dystrophy_type_2g https://www.malacards.org/card/muscular_dystrophy_limb_girdle_autosomal_recessive_7 Tcap autosomal recessive limb-girdle muscular dystrophy DOID:0110281 MEDGEN:400895 OMIM:601954 MONDO:0011170 TCAP autosomal recessive limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy caused by mutation in TCAP muscular dystrophy, limb-girdle, type 2G UMLS:C1866008 GARD:0010471 limb-girdle muscular dystrophy due to telethonin deficiency LGMD2G Autosomal recessive limb-girdle muscular dystrophy type 2G (LGMD2G) is a mild subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a variable onset (ranging from infancy to adolescence) of progressive proximal upper and lower limb muscle weakness and atrophy. Mild scapular winging, calf hypertrophy, and lack of respiratory and cardiac involvement are also observed. autosomal recessive limb-girdle muscular dystrophy caused by mutation in Tcap muscular dystrophy, limb-girdle, autosomal recessive 7 SCTID:720522001 Orphanet:34514 limb-girdle muscular dystrophy, type 2G MESH:C566599 autosomal recessive limb-girdle muscular dystrophy neuromuscular disease caused by qualitative or quantitative defects of telethonin