PomBase home

Disease association ontology term - MONDO:0700084 - myopathy caused by variation in GMPPB

Term summary

ID
MONDO:0700084
Name
myopathy caused by variation in GMPPB
Ontology or CV name
Disease association
Definition
Any myopathy in which the cause of the disease is a variation in the GMPPB gene.

Parents

Annotation

Disease association

MONDO:0014142 - autosomal recessive limb-girdle muscular dystrophy type 2T

References:

Genes:

MONDO:0014140 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14

References:

Genes:

MONDO:0014141 - muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14

References:

Genes: