Other hemoglobinopathies

Preferred Label : Other hemoglobinopathies;

Inclusion CIM-10 : Unstable hemoglobin hemolytic disease; Hb-E disease; Hb-C disease; Abnormal hemoglobin NOS; Hemoglobinopathy NOS; Congenital Heinz body anemia; Hb-D disease;

ICD-10 exclusion note : high-altitude polycythemia (D75.1); familial polycythemia (D75.0); other hemoglobinopathies with thalassemia (D56.8); Hb-M disease (D74.0); hereditary persistence of fetal hemoglobin [HPFH] (D56.4); methemoglobinemia (D74.-); hemoglobin E-beta thalassemia (D56.5);

Diag associé à un acte (%) : 71.1;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D582;

UMLS CUI

C0029632;

Automatic exact mappings (from CISMeF team)
- Hemoglobin disorders [LOINC component]
- Unstable hemoglobin disease (disorder) [SNOMED CT concept]
- hb C disease [MeSH concept]
- hb C disease [MeSH Supplementary Concept]
- hemoglobin C disease [DO Concept]
- hemoglobin D disease [DO Concept]
- hemoglobin E disease [DO Concept]
Currated CISMeF NLP mapping
- Other haemoglobinopathies [Vue CIM-11]
- Other haemoglobinopathies [MedDRA LLT]
- Other hemoglobinopathies [LOINC component]
DO Cross reference
- hemoglobin C disease [DO Concept]
- hemoglobin D disease [DO Concept]
- hemoglobin E disease [DO Concept]
- hemoglobinopathy [DO Concept]
ICD-10 exclusion(s)
- Congenital methemoglobinemia [ICD-10 Sub-category]
- Familial erythrocytosis [ICD-10 Sub-category]
- Hereditary persistence of fetal hemoglobin [HPFH] [ICD-10 Sub-category]
- Methemoglobinemia [ICD-10 category]
- Secondary polycythemia [ICD-10 Sub-category]
Manual NTBT mappings (CISMeF)
- Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome [ORDO Disease]
Orphanet concepts
- Beta-thalassemia associated with another hemoglobin anomaly [ORDO Disease]
- Beta-thalassemia with other manifestations [ORDO Disease]
- Heinz body anemia [ORDO Disease]
- Hemoglobin C disease [ORDO Disease]
- Hemoglobin C-beta-thalassemia syndrome [ORDO Disease]
- Hemoglobin D disease [ORDO Disease]
- Hemoglobin E disease [ORDO Disease]
- Hemoglobin E-beta-thalassemia syndrome [ORDO Disease]
- Hemoglobinopathy [ORDO Disease]
- Hemoglobinopathy Toms River [ORDO Disease]
- Unstable hemoglobin disease [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Other haemoglobinopathies [MedDRA LLT]
- Other haemoglobinopathies [Vue CIM-11]
- Other hemoglobinopathies [LOINC component]
- Other hemoglobinopathies [ICD-9 code]

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