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| Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v6.8 | TRIM32 | Ida Ertmanska Phenotypes for gene: TRIM32 were changed from Limb-Girdle Muscular Dystrophy, Recessive; Muscular dystrophy, limb-girdle, type 2H, 254110; Limb-girdle muscular dystrophy to Muscular dystrophy, limb-girdle, autosomal recessive 8, OMIM:254110; autosomal recessive limb-girdle muscular dystrophy type 2H, MONDO:0009683 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v6.7 | TRIM32 | Ida Ertmanska Publications for gene: TRIM32 were set to http://www.ncbi.nlm.nih.gov/books/NBK1408/ | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v6.6 | TRIM32 | Ida Ertmanska reviewed gene: TRIM32: Rating: GREEN; Mode of pathogenicity: None; Publications: 17994549, 30823891, 37217920, 40017290; Phenotypes: Muscular dystrophy, limb-girdle, autosomal recessive 8, OMIM:254110, autosomal recessive limb-girdle muscular dystrophy type 2H, MONDO:0009683; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||