Msh homeobox 2

Preferred Label : Msh homeobox 2;

Symbol : MSX2;

CISMeF acronym : MSX2;

Type : Gene;

Alternative titles and symbols : Muscle segment homeobox, drosophila, homolog of, 2; Msh, drosophila, homolog of, 2; MSX2;

Ensembl ID : ENSG00000120149;

Prefixed ID : *123101;

Details

Origin ID

123101;

UMLS CUI

C1417388;

Automatic exact mappings (from CISMeF team)
- msh homeobox 2 [ORDO Gene]
- msh homeobox 2 [HGNC gene]
HGNC gene
- msh homeobox 2 [HGNC gene]
ORDO concept(s)
- msh homeobox 2 [ORDO Gene]
Phenotypes related
- Craniosynostosis 2 [OMIM Phenotype]
- Parietal foramina 1 [OMIM Phenotype]
- Parietal foramina with cleidocranial dysplasia [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- msh homeobox 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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