Disease association ontology term - MONDO:0010671 - microphthalmia, syndromic 1
Term summary
ID
MONDO:0010671
Name
microphthalmia, syndromic 1
Ontology or CV name
Disease association
Parents
excluded_subClassOf
multiple congenital anomalies/dysmorphic syndrome-intellectual disability
excluded_subClassOf
microphthalmia, Lenz type
is_a
syndromic microphthalmia
is_a
NAA10-related syndrome
Annotation
Disease association
MONDO:0010671
-
microphthalmia, syndromic 1
References:
PB_REF:0000006
Genes:
naa10 (SPAC15E1.08)