Single lineage myelodysplasia
Basic details
Preferred term: Single lineage myelodysplasia
Alt. terms:
HPO term: Single lineage myelodysplasia
HPO code: HP:0012150
GenIA ID: 9040
Last updated on: 2021-08-02 21:50:33
Cross ref. with other ontologies
NCIT: -
MESH: -
EFO: -
OAE: -
SNOMEDCT: -
ICD10: -
Description
Abnormality/dysplasia of a single myeloid cell (erythroid, granulocytic, or megakaryocytic).
Hierarchical classification
PARENT terms
TERM
Single lineage myelodysplasia
CHILD terms
Reported patients added to GenIA DB
| SubjectID | Sex | Fam.ID | Age* | Population | MatchedTerm | Diagnosis | Reference & Pub.codes |
|---|---|---|---|---|---|---|---|
| 103485 | F | 215137 |
- | French | Myelodysplasia | Immunodeficiency 55 | PMID:28414293 [Fam.D:II.1(P5)] |
*Age: age reported at the first known time of manifestation; PMID: PubMed ID; GRID: GenIA reference ID (ref. not in PubMed).