Disease association ontology term - MONDO:0009485 - oculocerebrofacial syndrome, Kaufman type

Term summary

ID: MONDO:0009485
Name: oculocerebrofacial syndrome, Kaufman type
Ontology or CV name: Disease association

Parents

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

Annotation

Disease association

MONDO:0009485 - oculocerebrofacial syndrome, Kaufman type

References:

PB_REF:0000006

Genes:

hul5 (SPAC167.07c)