Disease association ontology term - MONDO:0014605 - Houge-Janssens syndrome 2
Term summary
ID
MONDO:0014605
Name
Houge-Janssens syndrome 2
Ontology or CV name
Disease association
Parents
excluded_subClassOf
syndromic intellectual disability
excluded_subClassOf
autosomal dominant non-syndromic intellectual disability
is_a
autosomal dominant disease
is_a
multiple congenital anomalies/dysmorphic syndrome-intellectual disability
is_a
Houge-Janssens syndrome
Annotation
Disease association
MONDO:0014605
-
Houge-Janssens syndrome 2
References:
PB_REF:0000006
Genes:
paa1 (SPAP8A3.09c)