msh homeobox 2

Preferred Label : msh homeobox 2;

Approved symbol HGNC : MSX2;

Name synonyms HGNC : craniosynostosis; type 2;

Alias symbols HGNC : CRS2; MSH; HOX8; PFM; FPP;

Chromosome HGNC : 5q35.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000120149;

Details

Origin ID

HGNC:7392;

UMLS CUI

C1417388;

Automatic exact mappings (from CISMeF team)
- Bristol Stool Type 2 [NCIt concept]
- Craniosynostosis [NCIt concept]
- Craniosynostosis [ICD-11 Subcategory]
- Craniosynostosis [PASCAL descriptor]
- Craniosynostosis [ORDO Disease]
- Craniosynostosis [MedDRA Preferred Term]
- Craniosynostosis [ICD-10 Sub-category]
- Craniosynostosis [HPO term]
- Craniosynostosis [OMIM phenotypic series]
- Craniosynostosis 2 [OMIM Phenotype]
- Craniosynostosis syndrome (disorder) [SNOMED CT concept]
- Msh homeobox 2 [OMIM gene]
- Type 2 (qualifier value) [SNOMED CT concept]
- craniofacial abnormalities [MedlinePlus Topic]
- craniosynostoses [MeSH Descriptor]
- craniosynostosis [Radlex concept]
- craniosynostosis [DO Concept]
- msh homeobox 2 [ORDO Gene]
OMIM gene
- Msh homeobox 2 [OMIM gene]
Orphanet gene
- msh homeobox 2 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Msh homeobox 2 [OMIM gene]

Keyword's position in hierarchy(ies) :

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