Disease association ontology term - MONDO:0859223 - congenital disorder of glycosylation, type Iw, autosomal dominant

Term summary

ID: MONDO:0859223
Name: congenital disorder of glycosylation, type Iw, autosomal dominant
Ontology or CV name: Disease association

Parents

is_a congenital disorder of glycosylation

Annotation

Disease association

MONDO:0859223 - congenital disorder of glycosylation, type Iw, autosomal dominant

References:

PB_REF:0000006

Genes:

stt3 (SPBC1271.02)