Disease #06601 (MYOPMIL (?Myopathy, congenital proximal, with minicore lesions), OMIM:618823)

Official abbreviation MYOPMIL
Name ?Myopathy, congenital proximal, with minicore lesions
OMIM ID 618823
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene FXR1
Associated tissues -
Disease features -
Remarks -

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