x chromosome-linked sideroblastic anemia, nos

Preferred Label : x chromosome-linked sideroblastic anemia, nos;

Origin ID

DC-14320;

UMLS CUI

C0221018;

Automatic exact mappings (from CISMeF team)
- Hereditary sideroblastic anemia (disorder) [Inactive SNOMED CT concept]
Currated CISMeF NLP mapping
- Anemia, sideroblastic, 1 [OMIM Phenotype]
- X chromosome-linked sideroblastic anemia (disorder) [SNOMED CT concept]
- X-linked sideroblastic anemia [ORDO Disease]
- X-linked sideroblastic anemia [MeSH concept]
- X-linked sideroblastic anemia [MeSH Supplementary Concept]
ICD-10 exact mapping(s)
- Other sideroblastic anaemias [ICD-10 Sub-category (who)]
Metaterm(s)
- hematology [CISMeF Metaterm]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Anemia, sideroblastic, 1 [OMIM Phenotype]
- Constitutional sideroblastic anemia [ORDO Disease]
- Hereditary Sideroblastic Anemia [NCIt concept]
- Hereditary sideroblastic anaemia [MedDRA Preferred Term]
- Hereditary sideroblastic anaemia [ICD-10 Sub-category (who)]
- Hereditary sideroblastic anaemias [ICD-11 Sub-sub category]
- Hereditary sideroblastic anemia [MedDRA LLT]
- Hereditary sideroblastic anemia [ICD-10 Sub-category]
- Hereditary sideroblastic anemia (disorder) [Inactive SNOMED CT concept]
- Hereditary syndromic sideroblastic anaemia [ICD-11 Sub-sub category]
- X-linked sideroblastic anemia [MeSH concept]
- X-linked sideroblastic anemia [ORDO Disease]