Diamond-Blackfan Anemia 9

Preferred Label : Diamond-Blackfan Anemia 9;

NCIt synonyms : DBA9;

NCIt definition : Congenital pure red cell aplasia caused by autosomal dominant mutation(s) in the RPS10 gene, encoding 40S ribosomal protein S10.;

Détails

Origin ID

C176918;

UMLS CUI

C2750081;

Currated CISMeF NLP mapping
- Diamond-Blackfan anemia 9 [MeSH Supplementary Concept]
- Diamond-Blackfan anemia 9 [MeSH concept]
- Diamond-Blackfan anemia 9 [DO Concept]
- Diamond-blackfan anemia 9 [OMIM Phenotype]
Has associated anatomic sites
- Bone Marrow [NCIt concept]
- Hematopoietic and Lymphatic System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Diamond-Blackfan anemia 9 [MeSH Supplementary Concept]
- Diamond-Blackfan anemia 9 [MeSH concept]
- Diamond-blackfan anemia 9 [OMIM Phenotype]
disease_has_finding
- Bone Marrow Failure [NCIt concept]
- Hereditary Lesion [NCIt concept]
- Marked Reduction or Absence of Erythroid Precursors in the Bone Marrow [NCIt concept]
- Reticulocytopenia [NCIt concept]
disease_has_molecular_abnormality
- RPS10 Gene Mutation [NCIt concept]
disease_has_normal_cell_origin
- Hematopoietic and Lymphoid Cell [NCIt concept]
disease_has_normal_tissue_origin
- Hematopoietic and Lymphoid Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Bone Marrow [NCIt concept]
- Hematopoietic and Lymphatic System [NCIt concept]
disease_mapped_to_gene
- RPS10 Gene [NCIt concept]
pathogenesis_of_disease_involves_gene
- RPS10 Gene [NCIt concept]
- RPS10 wt Allele [NCIt concept]
related_to_genetic_biomarker
- RPS10 Gene [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients