Disease association ontology term - MONDO:0014832 - intellectual disability, autosomal recessive 53
Term summary
ID
MONDO:0014832
Name
intellectual disability, autosomal recessive 53
Ontology or CV name
Disease association
Parents
excluded_subClassOf
autosomal recessive non-syndromic intellectual disability
is_a
congenital nervous system disorder
is_a
syndromic dyslipidemia
is_a
inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation
is_a
autosomal recessive syndromic intellectual disability
Annotation
Disease association
MONDO:0014832
-
intellectual disability, autosomal recessive 53
References:
PB_REF:0000006
Genes:
gpi7 (SPAC13G6.03)