Diamond-Blackfan Anemia 6

Preferred Label : Diamond-Blackfan Anemia 6;

NCIt synonyms : DBA6;

NCIt definition : Congenital pure red cell aplasia caused by autosomal dominant mutation(s) in the RPL5 gene, encoding 60S ribosomal protein L5.;

Details

Origin ID

C176915;

UMLS CUI

C2931850;

Currated CISMeF NLP mapping
- Aase Smith syndrome 2 [MeSH Supplementary Concept]
- Aase Smith syndrome 2 [MeSH concept]
- Diamond-Blackfan anemia 6 [DO Concept]
- Diamond-blackfan anemia 6 [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)
- Aase Smith syndrome 2 [MeSH Supplementary Concept]
- Aase Smith syndrome 2 [MeSH concept]
- Diamond-blackfan anemia 6 [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
- RPL5 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
- RPL5 Gene [NCIt concept]
pathogenesis_of_disease_involves_gene
- RPL5 Gene [NCIt concept]
- RPL5 wt Allele [NCIt concept]
related_to_genetic_biomarker
- RPL5 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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