Myelodysplasia
Basic details
Preferred term: Myelodysplasia
Alt. terms: Myelodysplastic syndrome | Hypoplastic myelodysplasia
HPO term: Myelodysplasia
HPO code: HP:0002863
GenIA ID: 454
Last updated on: 2021-12-10 17:55:48
Cross ref. with other ontologies
NCIT: -
MESH: -
EFO: -
OAE: -
SNOMEDCT: -
ICD10: D46.9
Description
Clonal hematopoietic stem cell disorders characterized by dysplasia (ineffective production) in one or more hematopoietic cell lineages, leading to anemia and cytopenia.
Hierarchical classification
PARENT terms
TERM
Myelodysplasia
Reported patients added to GenIA DB
| SubjectID | Sex | Fam.ID | Age* | Population | MatchedTerm | Diagnosis | Reference & Pub.codes |
|---|---|---|---|---|---|---|---|
| 101155 | M | 210235 | - | German | Hematological neoplasm | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:30250467 [JJ.II.I]; PMID:29729943 [Fam.JJ:II.1(83)]; PMID:34975878 [Fam.F098:P098] |
| 101160 | F | 211433 | - | Hematological neoplasm | Infantile-Onset Multisystem Autoimmune Disease 1 | PMID:34975878 [Fam.F101:P101] | |
| 101387 | M | 211537 | - | German | Hematological neoplasm | PMID:34975878 [Fam.F136:P136] | |
| 101462 | M | 210006 | - | Hematological neoplasm | Infantile-Onset Multisystem Autoimmune Disease 1 | PMID:34975878 [Fam.F154:P154] | |
| 101544 | F | 211170 | - | Hematological neoplasm | PMID:34975878 [Fam.F180:P180] | ||
| 101808 | F | 211441 | - | Hematological neoplasm | Immunodeficiency, common variable, 2 | PMID:34975878 [Fam.F265:P265] | |
| 101951 | M | 212062 | - | Hematological neoplasm | PMID:34975878 [Fam.F375:P375] | ||
| 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).