midline 1 - CISMeF

Preferred Label : midline 1;

Approved symbol HGNC : MID1;

Name synonyms HGNC : Opitz/BBB syndrome;

Alias symbols HGNC : OS; TRIM18; FXY; RNF59;

Chromosome HGNC : Xp22.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000101871;

Details

Origin ID

HGNC:7095;

UMLS CUI

C1417167;

Automatic exact mappings (from CISMeF team)
- E3 Ubiquitin-Protein Ligase Midline-1 [NCIt concept]
- Midline 1 [OMIM gene]
- hypertelorism with esophageal abnormality and hypospadias [MeSH Supplementary Concept]
- midline 1 [ORDO Gene]
NCIt concept
- MID1 Gene [NCIt concept]
OMIM gene
- Midline 1 [OMIM gene]
Orphanet gene
- midline 1 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MID1 Gene [NCIt concept]
- Midline 1 [OMIM gene]

Keyword's position in hierarchy(ies) :

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