Disease association ontology term - MONDO:0000181 - microcephaly and chorioretinopathy

Term summary

ID: MONDO:0000181
Name: microcephaly and chorioretinopathy
Ontology or CV name: Disease association

Parents

is_a microcephaly
is_a chorioretinitis
is_a Mendelian neurodevelopmental disorder

Annotation

Disease association

MONDO:0009624 - microcephaly and chorioretinopathy 1

References:

PB_REF:0000006

Genes:

alp16 (SPCC4G3.19)

MONDO:0014592 - microcephaly and chorioretinopathy 3

References:

PB_REF:0000006

Genes:

gfh1 (SPBC211.06)