Disease #06727 (LGMDR26 (dystrophy, muscular, limb-girdle, autosomal recessive, type 26), OMIM:618848)

Official abbreviation LGMDR26
Name dystrophy, muscular, limb-girdle, autosomal recessive, type 26
OMIM ID 618848
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene POPDC3
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited 2024-01-10 22:25:07 +01:00 (CET)


Individuals

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00466377 - Pending - F - France - - - - - LGMDR26 - - POPDC3 1 1 Camille Verebi
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