Sickle cell disease without crisis

ICD-11 code : 3A51.1;

Preferred Label : Sickle cell disease without crisis;

ICD-11 definition : A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may present with fatigue, shortness of breath, dizziness, headaches, pallor of skin or mucous membranes, and jaundice. This disorder is confirmed by identification of HbS mutation by genetic testing.;

ICD-11 synonym : Hb-SS disease without crisis; HbSS without crisis; Sickle-cell anaemia without crisis; SCD - [sickle cell disease]; SCA - [sickle cell anaemia]; sickle cell disease NOS; drepanocytosis; sickle cell anaemia; sickle cell disease;

ICD-11 acronym : SCA; SCD;

ICD-11 inclusion : sickle cell nephropathy; drepanocytic anaemia; sickling disorder due to haemoglobin S; sickle-cell haemoglobin disease; herrick anaemia; sickle-cell disorder NOS; Hb S disease; drepanocythemia; Hb SS disease; haemoglobin S disease; haemoglobin SS disease; sickle cell syndrome; sickle cell disorder; hereditary haemoglobinopathy disorder homozygous for haemoglobin S; Sickle-cell anaemia NOS;

Details

Origin ID

1711513381;

UMLS CUI

C0272078;

Automatic exact mappings (from CISMeF team)
- Abdominal compartment syndrome [MedDRA Preferred Term]
- Acyl-CoA Desaturase [NCIt concept]
- Cardiac conduction defect [OMIM Phenotype]
- Carnitine deficiency, systemic primary [OMIM Phenotype]
- Doctor of Science [NCIt concept]
- Hb-SS disease without crisis [ICD-9 code]
- Hemoglobin SS disease with crisis (disorder) [SNOMED CT concept]
- IFL protocol [MeSH Supplementary Concept]
- SCD Gene [NCIt concept]
- Schnyder corneal dystrophy [ORDO Disease]
- Schnyder corneal dystrophy [OMIM Phenotype]
- Sickle cell anemia with crisis [MedDRA LLT]
- Sickle cell disease [MedDRA Preferred Term]
- Sickle cell trait (disorder) [SNOMED CT concept]
- Sickle-cell disease without crisis [ICD-10 Sub-category]
- Stearoyl-coa desaturase [OMIM gene]
- Sudden Cardiac Death [NCIt concept]
- Superior Cerebellar Artery [NCIt concept]
- acute coronary syndrome [MeSH Descriptor]
- cardiac arrest [MedlinePlus Topic]
- solute carrier family 22 member 5 [ORDO Gene]
Currated CISMeF NLP mapping
- Anaemia sickle cell [MedDRA LLT]
- Anemia sickle cell [MedDRA LLT]
- Drepanocytosis [MedDRA LLT]
- Hemoglobin SS disease without crisis (disorder) [SNOMED CT concept]
- Sickle Cell Disease [NCIt concept]
- Sickle cell anaemia [MedDRA Preferred Term]
- Sickle cell anemia [ORDO Disease]
- Sickle cell anemia [LOINC component]
- Sickle cell anemia [PASCAL descriptor]
- Sickle cell disease [OMIM Phenotype]
- Sickle cell disease [MedDRA LLT]
- Sickle cell disease NOS [MedDRA LLT]
- Sickle cell-hemoglobin SS disease (disorder) [SNOMED CT concept]
- anemia, sickle cell [MeSH concept]
- anemia, sickle cell [MeSH Descriptor]
- hemoglobin s disease [SNOMED Notion]
- sickle cell anemia [Radlex concept]
- sickle cell anemia [DO Concept]
- sickle cell disease [MedlinePlus Topic]
- sickle cell disease [Blood Transfusion thesaurus concept]
ICD-10 Mapping
- Sickle-cell disease without crisis [ICD-10 Sub-category]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hb-SS disease without crisis [ICD-9 code]
- Hemoglobin SS disease without crisis (disorder) [SNOMED CT concept]
- Sickle-cell disease without crisis [ICD-10 Sub-category]
- hemoglobin s disease without crisis [SNOMED Notion]
Validated automatic mappings to BTNT
- Sickling disorder due to hemoglobin S (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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