Heart, malformation of

Preferred Label : Heart, malformation of;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant vs. multifactorial;

Prefixed ID : 140500;

Details

Origin ID

140500;

UMLS CUI

C0018798;

Automatic exact mappings (from CISMeF team)
- Structural developmental anomaly of heart or great vessels [Bloc CIM-11]
- congenital heart disease [DO Concept]
- obsolete Malformation of the heart and great vessels [HPO term]
Currated CISMeF NLP mapping
- HEART MALFORMATION [WHO-ART High Level Term]
- Heart Malformation [NCIt concept]
- Heart malformation [MedDRA LLT]
- Malformation heart (NOS) [MedDRA LLT]
- congenital heart malformation [Disease (Nov.)]
- heart defects, congenital [MeSH Descriptor]
- heart malformation [BNCI symptom]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Hypoplastic left heart [HPO term]
- Multifactorial inheritance [HPO term]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Abnormal heart morphology [HPO term]
- Anomaly heart [MedDRA LLT]
- Congenital malformation of heart, unspecified [ICD-10 Sub-category (who)]
- Congenital malformation of heart, unspecified [ICD-10 Sub-category]
- HEART MALFORMATION [WHO-ART High Level Term]
- Heart Malformation [NCIt concept]
- Heart malformation [MedDRA LLT]
- Malformation heart (NOS) [MedDRA LLT]
- Rare congenital non-syndromic heart malformation [ORDO Disease]
- Unspecified congenital anomaly of heart [ICD-9 code]
- Unspecified congenital anomaly of heart [MedDRA LLT]
- congenital heart defects [MedlinePlus Topic]
- congenital heart disease [DO Concept]
- heart defects, congenital [MeSH Descriptor]
- heart defects, congenital [MeSH concept]
- heart malformation [BNCI symptom]

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