Disease association ontology term - MONDO:0009598 - metaphyseal chondrodysplasia-retinitis pigmentosa syndrome

Term summary

ID: MONDO:0009598
Name: metaphyseal chondrodysplasia-retinitis pigmentosa syndrome
Ontology or CV name: Disease association

Parents

is_a syndromic disease
is_a osteochondrodysplasia

Annotation

Disease association

MONDO:0009598 - metaphyseal chondrodysplasia-retinitis pigmentosa syndrome

References:

PB_REF:0000006

Genes:

cyp7 (SPBC16H5.05c)