Hereditary sideroblastic anemia

Preferred Label : Hereditary sideroblastic anemia;

Inclusion CIM-10 : Sex-linked hypochromic sideroblastic anemia;

Diag associé à un acte (%) : 85.7;

Autres : 2;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D640;

UMLS CUI

C0221018;

Automatic exact mappings (from CISMeF team)
- Anemia, sideroblastic, 1 [OMIM Phenotype]
Currated CISMeF NLP mapping
- 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 (disorder) [Inactive SNOMED CT concept]
- Hereditary syndromic sideroblastic anaemia [ICD-11 Sub-sub category]
- hereditary sideroblastic anemia, nos [SNOMED Notion]
Excluded by
- Disorders of iron metabolism [ICD-10 Sub-category]
Orphanet concepts
- Adult-onset autosomal recessive sideroblastic anemia [ORDO Disease]
- Autosomal recessive sideroblastic anemia [ORDO Disease]
- Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome [ORDO Disease]
- Constitutional sideroblastic anemia [ORDO Disease]
- Pearson syndrome [ORDO Disease]
- Severe congenital hypochromic anemia with ringed sideroblasts [ORDO Disease]
- Sideroblastic anemia [ORDO Disease]
- X-linked sideroblastic anemia [ORDO Disease]
- X-linked sideroblastic anemia and spinocerebellar ataxia [ORDO Disease]
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 anaemias [ICD-11 Sub-sub category]
- Hereditary sideroblastic anemia [MedDRA LLT]
- 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]
- hereditary sideroblastic anemia, nos [SNOMED Notion]
- x chromosome-linked sideroblastic anemia, nos [SNOMED Notion]

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