Disease #02405 (LGMDR7;LGMD2G (dystrophy, muscular, limb-girdle, type 2G), OMIM:601954)

Official abbreviation LGMDR7;LGMD2G
Name dystrophy, muscular, limb-girdle, type 2G
OMIM ID 601954
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene TCAP
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-01-19 16:08:09 +01:00 (CET)


Individuals

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00213419 Fa,F50-1 PubMed: Francis 2014 4-generation family, 3 affected (2F, M), unaffected heterozygous carrier parents/relatives M yes India Dravidian - - - - LGMDR7;LGMD2G see paper; ..., CPK 3729 TCAP TCAP 1 3 Francis Amirtharaj
00213420 FamF97-1 PubMed: Francis 2014 5-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M yes India Dravidian - - - - LGMDR7;LGMD2G see paper; ..., CPK 1583 TCAP TCAP 1 1 Francis Amirtharaj
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