Disease #06997 (MMCKR (myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis), OMIM:620138)

Official abbreviation MMCKR
Name myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis
OMIM ID 620138
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene MLIP
Associated tissues -
Disease features myopathy, myalgia, increased serum creatine kinase, with/without episodic rhabdomyolysis
Remarks -
Date created 2023-01-19 15:25:33 +01:00 (CET)
Date last edited N/A

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