cono-truncal heart malformation

Preferred Label : cono-truncal heart malformation;

Obsolete resource : true;

Approved symbol HGNC : CTHM;

Chromosome HGNC : 22q11;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:2502;

UMLS CUI

C1413793;

Automatic exact mappings (from CISMeF team)
- Conotruncal heart malformations [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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