dyserythropoiesis, congenital, with internuclear chromatin bridges and ultrastructurally normal erythroblast heterochromatin

Preferred Label : dyserythropoiesis, congenital, with internuclear chromatin bridges and ultrastructurally normal erythroblast heterochromatin;

Origin ID

C566368;

UMLS CUI

C1863768;

CISMeF manual mappings
- Dyserythropoiesis, congenital, with ultrastructurally normal erythroblast heterochromatin [OMIM Phenotype]
MeSH term(s) associated for indexing
- anemia [MeSH Descriptor]
- erythrocytes, abnormal [MeSH Descriptor]
Record concept(s)
- dyserythropoiesis, congenital, with internuclear chromatin bridges and ultrastructurally normal erythroblast heterochromatin [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]