Smad family member 2

Preferred Label : Smad family member 2;

Symbol : SMAD2;

CISMeF acronym : SMAD2;

Type : Gene;

Alternative titles and symbols : Mothers against decapentaplegic, drosophila, homolog of, 2; Sma- and mad-related protein 2 mad, drosophila, homolog of; MADH2; MADR2;

Ensembl ID : ENSG00000175387;

Prefixed ID : *601366;

Détails

Origin ID

601366;

UMLS CUI

C1334468;

Automatic exact mappings (from CISMeF team)
- Mothers Against Decapentaplegic Homolog 2 [NCIt concept]
- SMAD family member 2 [HGNC gene]
- SMAD2 Gene [NCIt concept]
- SMAD2 wt Allele [NCIt concept]
HGNC gene
- SMAD family member 2 [HGNC gene]
NCIt concept(s)
- Mothers Against Decapentaplegic Homolog 2 [NCIt concept]
- SMAD2 Gene [NCIt concept]
- SMAD2 wt Allele [NCIt concept]
ORDO concept(s)
- SMAD family member 2 [ORDO Gene]
Phenotypes related
- Congenital heart defects, multiple types, 8, with or without heterotaxy [OMIM Phenotype]
- Loeys-dietz syndrome 6 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SMAD family member 2 [HGNC gene]
- SMAD2 Gene [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients