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Disease association ontology term - MONDO:0014806 - spinal muscular atrophy with congenital bone fractures 1

Term summary

ID
MONDO:0014806
Name
spinal muscular atrophy with congenital bone fractures 1
Ontology or CV name
Disease association
Definition
Any prenatal-onset spinal muscular atrophy with congenital bone fractures in which the cause of the disease is a mutation in the TRIP4 gene.

Parents

Annotation

Disease association

MONDO:0014806 - spinal muscular atrophy with congenital bone fractures 1

References:

Genes: