tectonic family member 2

Preferred Label : tectonic family member 2;

Approved symbol HGNC : TCTN2;

Name synonyms HGNC : type 8; Meckel syndrome;

Alias symbols HGNC : TECT2; MKS8; JBTS24; FLJ12975;

Chromosome HGNC : 12q24.31;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000168778;

Details

Origin ID

HGNC:25774;

UMLS CUI

C1824359;

Automatic exact mappings (from CISMeF team)
- Meckel syndrome [PASCAL descriptor]
- Meckel syndrome [ORDO Disease]
- Meckel syndrome [DO Concept]
- Meckel syndrome [OMIM phenotypic series]
- Meckel syndrome, type 1 [OMIM Phenotype]
- Meckel syndrome, type 8 [OMIM Phenotype]
- Meckel-Gruber syndrome [ICD-11 Sub-sub category]
- Tectonic family, member 2 [OMIM gene]
- meckel syndrome type 1 [MeSH Supplementary Concept]
- tectonic family member 2 [ORDO Gene]
OMIM gene
- Tectonic family, member 2 [OMIM gene]
Orphanet gene
- tectonic family member 2 [ORDO Gene]
See also inter- (CISMeF)
- Joubert syndrome 24 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Tectonic family, member 2 [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients