Disease association ontology term - MONDO:0007677 - hyperglycinuria
Term summary
ID
MONDO:0007677
Name
hyperglycinuria
Ontology or CV name
Disease association
Parents
is_a
urinary system disorder
is_a
hereditary disease
Annotation
Disease association
MONDO:0007677
-
hyperglycinuria
References:
PB_REF:0000006
Genes:
avt3 (SPAC3H1.09c)