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

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

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0566668;

UMLS CUI

C1863768;

CISMeF manual mappings
- Dyserythropoiesis, congenital, with ultrastructurally normal erythroblast heterochromatin [OMIM Phenotype]
Related record
- dyserythropoiesis, congenital, with internuclear chromatin bridges and ultrastructurally normal erythroblast heterochromatin [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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