Transmembrane protein 216

Preferred Label : Transmembrane protein 216;

Symbol : TMEM216;

CISMeF acronym : TMEM216;

Type : Gene;

Ensembl ID : ENSG00000187049;

Prefixed ID : *613277;

Details

Origin ID

613277;

UMLS CUI

C2680482;

Automatic exact mappings (from CISMeF team)
- Transmembrane Protein 216 [NCIt concept]
Currated CISMeF NLP mapping
- TMEM216 Gene [NCIt concept]
- TMEM216 gene [LOINC component]
- transmembrane protein 216 [ORDO Gene]
- transmembrane protein 216 [HGNC gene]
HGNC gene
- transmembrane protein 216 [HGNC gene]
NCIt concept(s)
- TMEM216 Gene [NCIt concept]
- TMEM216 wt Allele [NCIt concept]
- Transmembrane Protein 216 [NCIt concept]
ORDO concept(s)
- transmembrane protein 216 [ORDO Gene]
Phenotypes related
- Joubert syndrome 2 [OMIM Phenotype]
- Meckel syndrome, type 2 [OMIM Phenotype]
- Retinitis pigmentosa 98 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- TMEM216 Gene [NCIt concept]
- TMEM216 gene [LOINC component]
- transmembrane protein 216 [HGNC gene]

Keyword's position in hierarchy(ies) :

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