Ostium Primum Defect

Preferred Label : Ostium Primum Defect;

NCIt definition : A congenital defect in the atrial septum at the level of the atrioventricular valves, resulting in abnormalities in the mitral and/or tricuspid valve; this defect is most commonly seen in those with Trisomy 21.;

Details

Origin ID

C34921;

UMLS CUI

C0031192;

Automatic exact mappings (from CISMeF team)
- Ostium primum defect [ICD-9 code]
- Primum atrial septal defect [HPO term]
- heart septal defects, atrial [MeSH Descriptor]
Currated CISMeF NLP mapping
- Atrial septal defect, ostium primum type [ORDO Disease]
- Ostium primum defect [MedDRA LLT]
- Ostium primum defect (disorder) [SNOMED CT concept]
- ostium primum defect [SNOMED Notion]
- persistent ostium primum [MeSH concept]
Has associated anatomic sites
- Cardiovascular System [NCIt concept]
- Heart [NCIt concept]
- Respiratory System [NCIt concept]
- Thoracic Cavity [NCIt concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Ostium primum [FMA entity]
- Ostium primum defect [MedDRA LLT]
- Ostium primum defect [ICD-9 code]
- Ostium primum defect (disorder) [SNOMED CT concept]
- ostium primum defect [SNOMED Notion]
- persistent ostium primum [MeSH concept]

Keyword's position in hierarchy(ies) :

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