Disease #07061 (LGMDR27 (dystrophy, muscular, limb-girdle, autosomal recessive, type 27), OMIM:619566)

Official abbreviation LGMDR27
Name dystrophy, muscular, limb-girdle, autosomal recessive, type 27
OMIM ID 619566
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene JAG2
Associated tissues -
Disease features -
Remarks -
Date created 2024-01-12 21:16:14 +01:00 (CET)
Date last edited N/A


Individuals

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00454929 - - - - - France - - - - - LGMDR27 - - JAG2 2 1 Svetlana Gorokhova
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