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

Official abbreviation PGBM-2
Name myopathy, polyglucosan body, type 2 (PGBM-2)
OMIM ID 616199
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene GYG1
Associated tissues -
Disease features -
Remarks -