Disease association ontology term - MONDO:0010441 - CK syndrome
Term summary
ID
MONDO:0010441
Name
CK syndrome
Ontology or CV name
Disease association
Parents
is_a
syndromic intellectual disability
is_a
disorder of development or morphogenesis
is_a
Mendelian neurodevelopmental disorder
Annotation
Disease association
MONDO:0010441
-
CK syndrome
References:
PB_REF:0000006
Genes:
erg26 (SPBC3F6.02c)