Matrilin 3 - CISMeF

Preferred Label : Matrilin 3;

Symbol : MATN3;

CISMeF acronym : MATN3;

Type : Gene;

Ensembl ID : ENSG00000132031;

Prefixed ID : *602109;

Détails

Origin ID

602109;

UMLS CUI

C1417043;

Automatic exact mappings (from CISMeF team)
- matrilin 3 [ORDO Gene]
- matrilin 3 [HGNC gene]
- matrilin proteins [MeSH Descriptor]
HGNC gene
- matrilin 3 [HGNC gene]
ORDO concept(s)
- matrilin 3 [ORDO Gene]
Phenotypes related
- Epiphyseal dysplasia, multiple, 5 [OMIM Phenotype]
- Osteoarthritis susceptibility 2 [OMIM Phenotype]
- Spondyloepimetaphyseal dysplasia, borochowitz-cormier-daire type [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- matrilin 3 [HGNC gene]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients