Malonyl-coa decarboxylase

Preferred Label : Malonyl-coa decarboxylase;

Symbol : MLYCD;

CISMeF acronym : MLYCD;

Type : Gene;

Alternative titles and symbols : MCD;

Ensembl ID : ENSG00000103150;

Prefixed ID : *606761;

Details

Origin ID

606761;

UMLS CUI

C1417196;

Automatic exact mappings (from CISMeF team)
- MUC1 wt Allele [NCIt concept]
- Macular corneal dystrophy [ORDO Disease]
- Malonyl-CoA decarboxylase (substance) [SNOMED CT concept]
- Multicentric Castleman disease [ORDO Disease]
- Multiple carboxylase deficiency [ORDO Disease]
- macular dystrophy, corneal type 1 [MeSH Supplementary Concept]
- malonyl-CoA decarboxylase [ORDO Gene]
- malonyl-CoA decarboxylase [HGNC gene]
- malonyl-CoA decarboxylase [MeSH concept]
- malonyl-CoA decarboxylase [MeSH Supplementary Concept]
- malonyl-coa decarboxylase [SNOMED Notion]
- mucin 1, cell surface associated [ORDO Gene]
- multicentric Castleman disease [DO Concept]
HGNC gene
- malonyl-CoA decarboxylase [HGNC gene]
ORDO concept(s)
- malonyl-CoA decarboxylase [ORDO Gene]
Phenotypes related
- Malonyl-coa decarboxylase deficiency [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MLYCD gene [LOINC component]
- malonyl-CoA decarboxylase [HGNC gene]

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