Disease association ontology term - MONDO:0013851 - autosomal dominant aplasia and myelodysplasia

Term summary

ID: MONDO:0013851
Name: autosomal dominant aplasia and myelodysplasia
Ontology or CV name: Disease association

Parents

is_a bone marrow failure syndrome
is_a inherited aplastic anemia

Annotation

Disease association

MONDO:0013851 - autosomal dominant aplasia and myelodysplasia

References:

PB_REF:0000006

Genes:

srp72 (SPCC320.10)