Wingless-type mmtv integration site family, member 10a

Preferred Label : Wingless-type mmtv integration site family, member 10a;

Symbol : WNT10A;

CISMeF acronym : WNT10A;

Type : Gene;

Ensembl ID : ENSG00000135925;

Prefixed ID : *606268;

Details

Origin ID

606268;

UMLS CUI

C1422222;

Automatic exact mappings (from CISMeF team)
- Protein Wnt-10a [NCIt concept]
- WNT10A Gene [NCIt concept]
- Wnt family member 10A [ORDO Gene]
- Wnt family member 10A [HGNC gene]
HGNC gene
- Wnt family member 10A [HGNC gene]
NCIt concept(s)
- Protein Wnt-10a [NCIt concept]
- WNT10A Gene [NCIt concept]
- WNT10A wt Allele [NCIt concept]
ORDO concept(s)
- Wnt family member 10A [ORDO Gene]
Phenotypes related
- Odontoonychodermal dysplasia [OMIM Phenotype]
- Schopf-schulz-passarge syndrome [OMIM Phenotype]
- Tooth agenesis, selective, 4 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- WNT10A Gene [NCIt concept]
- Wnt family member 10A [HGNC gene]

Keyword's position in hierarchy(ies) :

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