Disease #04497 (PGBM2 (myopathy, polyglucosan body, type 2 (PGBM-2)), OMIM:616199)

Official abbreviation PGBM2
Name myopathy, polyglucosan body, type 2 (PGBM-2)
OMIM ID 616199
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 GYG1
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00472253 - Verebi et al. (submitted) - M - France - - - - - PGBM2 0003198: Myopathy, 0003376: Steppage gait, 0003391: Gowers' sign - GYG1 2 1 Camille Verebi
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