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Disease association ontology term - MONDO:0700070 - myopathy caused by variation in POMT1

Term summary

ID
MONDO:0700070
Name
myopathy caused by variation in POMT1
Ontology or CV name
Disease association
Definition
Any myopathy in which the cause of the disease is a variation in the POMT1 gene.

Parents

Annotation

Disease association

MONDO:0012248 - autosomal recessive limb-girdle muscular dystrophy type 2K

References:

Genes:

MONDO:0009364 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1

References:

Genes:

MONDO:0013159 - muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1

References:

Genes: