Disease #00213 (612954 (MYOPATHY, MYOFIBRILLAR, 6), OMIM:612954)

Official abbreviation 612954
Name MYOPATHY, MYOFIBRILLAR, 6
OMIM ID 612954
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2024-09-06 10:55:15 +00:00 (UTC)
Date last edited N/A

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