Disease association ontology term - MONDO:0030261 - pontocerebellar hypoplasia, type 1F

Term summary

ID: MONDO:0030261
Name: pontocerebellar hypoplasia, type 1F
Ontology or CV name: Disease association

Parents

is_a pontocerebellar hypoplasia

Annotation

Disease association

MONDO:0030261 - pontocerebellar hypoplasia, type 1F

References:

PB_REF:0000006

Genes:

csl4 (SPCC1840.11)