Map kinase-activating death domain

Preferred Label : Map kinase-activating death domain;

Symbol : MADD;

CISMeF acronym : MADD;

Type : Gene;

Alternative titles and symbols : Differentially expressed in normal and neoplastic cells; Insulinoma-glucagonoma protein 20; Rab3 gdp/gtp exchange protein; DENN; IG20; RAB3GEP; KIAA0358;

Ensembl ID : ENSG00000110514;

Prefixed ID : *603584;

Details

Origin ID

603584;

UMLS CUI

C1366909;

Automatic exact mappings (from CISMeF team)
- ETFA wt Allele [NCIt concept]
- MADD Gene [NCIt concept]
- MADD wt Allele [NCIt concept]
- MAP Kinase-Activating Death Domain Protein [NCIt concept]
- MAP kinase activating death domain [HGNC gene]
- Mixed anxiety and depressive disorder (disorder) [SNOMED CT concept]
- Multiple acyl-CoA dehydrogenase deficiency [ORDO Disease]
- Multiple acyl-CoA dehydrogenase deficiency [ICD-11 More detail]
- electron transfer flavoprotein subunit alpha [ORDO Gene]
- electron transfer flavoprotein subunit alpha [HGNC gene]
- monoacetyldapsone [MeSH Supplementary Concept]
- multiple acyl-CoA dehydrogenase deficiency [DO Concept]
HGNC gene
- MAP kinase activating death domain [HGNC gene]
NCIt concept(s)
- MADD Gene [NCIt concept]
- MADD wt Allele [NCIt concept]
- MAP Kinase-Activating Death Domain Protein [NCIt concept]
ORDO concept(s)
- MAP kinase activating death domain [ORDO Gene]
Phenotypes related
- Deeah syndrome [OMIM Phenotype]
- Neurodevelopmental disorder with dysmorphic facies, impaired speech, and hypotonia [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MADD Gene [NCIt concept]
- MAP kinase activating death domain [HGNC gene]

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