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Disease association ontology term - MONDO:0016195 - neuromuscular disease caused by qualitative or quantitative defects of beta-myosin heavy chain (MYH7)

Term summary

ID
MONDO:0016195
Name
neuromuscular disease caused by qualitative or quantitative defects of beta-myosin heavy chain (MYH7)
Ontology or CV name
Disease association

Parents

Annotation

Disease association

MONDO:0008409 - congenital myopathy 7A, myosin storage, autosomal dominant

References:

Genes:

MONDO:0008050 - MYH7-related skeletal myopathy

References:

Genes: