Disease #00133 (MFM9 (MYOPATHY, MYOFIBRILLAR, 9, WITH EARLY RESPIRATORY FAILURE), OMIM:603689)

Official abbreviation MFM9
Name MYOPATHY, MYOFIBRILLAR, 9, WITH EARLY RESPIRATORY FAILURE
OMIM ID 603689
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TTN
Associated tissues -
Disease features -
Remarks -

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