Wingless-type mmtv integration site family, member 7a

Preferred Label : Wingless-type mmtv integration site family, member 7a;

Symbol : WNT7A;

CISMeF acronym : WNT7A;

Type : Gene;

Ensembl ID : ENSG00000154764;

Prefixed ID : *601570;

Details

Origin ID

601570;

UMLS CUI

C1337005;

Automatic exact mappings (from CISMeF team)
- Protein Wnt-7a [NCIt concept]
- WNT7A Gene [NCIt concept]
- Wnt family member 7A [ORDO Gene]
- Wnt family member 7A [HGNC gene]
HGNC gene
- Wnt family member 7A [HGNC gene]
NCIt concept(s)
- Protein Wnt-7a [NCIt concept]
- WNT7A Gene [NCIt concept]
- WNT7A wt Allele [NCIt concept]
ORDO concept(s)
- Wnt family member 7A [ORDO Gene]
Phenotypes related
- Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly [OMIM Phenotype]
- Ulna and fibula, absence of, with severe limb deficiency [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- WNT7A Gene [NCIt concept]
- Wnt family member 7A [HGNC gene]

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