Disease association ontology term - MONDO:0044634 - retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome

Term summary

ID: MONDO:0044634
Name: retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome
Ontology or CV name: Disease association

Parents

is_a syndromic disease
is_a hereditary disease
is_a multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome

Annotation

Disease association

MONDO:0044634 - retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome

References:

Genes:

rrp4 (SPAC2F7.14c)