Disease association ontology term - MONDO:0013968 - PGM1-congenital disorder of glycosylation
Term summary
ID
MONDO:0013968
Name
PGM1-congenital disorder of glycosylation
Ontology or CV name
Disease association
Parents
is_a
congenital disorder of glycosylation type I
is_a
familial dilated cardiomyopathy
is_a
disorder of protein N-glycosylation
Annotation
Disease association
MONDO:0013968
-
PGM1-congenital disorder of glycosylation
References:
PB_REF:0000006
Genes:
pgm1 (SPBC32F12.10)