Disease #04288 (LGMDD2;LGMD1F (dystrophy, muscular, limb-girdle, autosomal dominant, type 2 (LGMD1F)), OMIM:608423)

Official abbreviation LGMDD2;LGMD1F
Name dystrophy, muscular, limb-girdle, autosomal dominant, type 2 (LGMD1F)
OMIM ID 608423
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene TNPO3
Associated tissues -
Disease features -
Remarks -
Date created 2015-06-19 22:24:12 +02:00 (CEST)
Date last edited 2024-01-12 20:56:41 +01:00 (CET)


Individuals

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00436410 269670 - - M no Germany - - - - - LGMDD2;LGMD1F Myofibrillar myopathy TNPO3 TNPO3 1 1 Andreas Laner
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