Microcephaly - CISMeF

Preferred Label : Microcephaly;

Code considérée comme une complication de niveau 2, 3 ou 4 : 2;

Diag associé à un acte (%) : 84;

Details

Origin ID

Q02;

Automatic exact mappings (from CISMeF team)
- Congenital anomaly of neurological system [ICPC-3 diagnosis]
- hydromicrocephaly [SNOMED Notion]
Currated CISMeF NLP mapping
- MICROCEPHALY [WHO-ART High Level Term]
- Microcephalic [MedDRA LLT]
- Microcephalus [ICD-9 code]
- Microcephalus [MedDRA LLT]
- Microcephalus (disorder) [SNOMED CT concept]
- Microcephaly [MedDRA Preferred Term]
- Microcephaly [PASCAL descriptor]
- Microcephaly [ICD-10 category]
- Microcephaly [NCIt concept]
- Microcephaly [HPO term]
- Microcephaly [HRDO Sign]
- Microencephaly [MedDRA Preferred Term]
- microcephalus [SNOMED Notion]
- microcephaly [Disease (Nov.)]
- microcephaly [DO Concept]
- microcephaly [MeSH Descriptor]
- microcephaly [MeSH concept]
Exclusion CIM-10
- Cystic kidney disease, unspecified [ICD-10 Sub-category (who)]
Exclusion(s) CIM-10
- Other congenital malformations of skull and face bones [ICD-10 category (who)]
HRDO close match(es)
- Autosomal dominant primary microcephaly [ORDO Disease]
- Autosomal recessive primary microcephaly [ORDO Disease]
Metaterm(s)
- neonatology [CISMeF Metaterm]
SNOMED int. exact match(es)
- hydromicrocephaly [SNOMED Notion]
- microcephalus [SNOMED Notion]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Isolated congenital microcephaly [ORDO Disease]
- MICROCEPHALY [WHO-ART High Level Term]
- Microcephalic [MedDRA LLT]
- Microcephalus [ICD-9 code]
- Microcephalus [MedDRA LLT]
- Microcephalus (disorder) [SNOMED CT concept]
- Microcephaly [MedDRA Preferred Term]
- Microcephaly [HRDO Sign]
- Microcephaly [NCIt concept]
- Microencephaly [MedDRA Preferred Term]
- microcephalus [SNOMED Notion]
- microcephaly [MeSH Descriptor]
- microcephaly [MeSH concept]

Keyword's position in hierarchy(ies) :

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