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Disease association ontology term - MONDO:0014542 - congenital myasthenic syndrome 15

Term summary

ID
MONDO:0014542
Name
congenital myasthenic syndrome 15
Ontology or CV name
Disease association
Definition
Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the ALG14 gene.

Parents

Annotation

Disease association

MONDO:0014542 - congenital myasthenic syndrome 15

References:

Genes: