Membrane metalloendopeptidase

Preferred Label : Membrane metalloendopeptidase;

Symbol : MME;

CISMeF acronym : MME;

Type : Gene;

Alternative titles and symbols : Common acute lymphocytic leukemia antigen; Neutral endopeptidase, membrane-associated; CALLA; CD10; NEPRILYSIN; NEP; ENKEPHALINASE; ATRIOPEPTIDASE;

Ensembl ID : ENSG00000196549;

Prefixed ID : *120520;

Details

Origin ID

120520;

UMLS CUI

C1366499;

Automatic exact mappings (from CISMeF team)
- CD10 [LOINC component]
- CD10 Ag [LOINC component]
- CD10 Expressing Cell Count [NCIt concept]
- Calla (organism) [SNOMED CT concept]
- DDR1 wt Allele [NCIt concept]
- Lymphocyte antigen CD10 (substance) [SNOMED CT concept]
- MME [MeSH concept]
- MME [MeSH Supplementary Concept]
- MME Gene [NCIt concept]
- MME wt Allele [NCIt concept]
- Master of Mechanical Engineering [NCIt concept]
- Milligram Morphine Equivalent [NCIt concept]
- Multimodal Education [NCIt concept]
- Nepali Language [NCIt concept]
- Neprilysin [NCIt concept]
- Oral Morphine Milligram Equivalents [NCIt concept]
- membrane metallo-endopeptidase [SNOMED Notion]
- membrane metalloendopeptidase [ORDO Gene]
- membrane metalloendopeptidase [HGNC gene]
- neprilysin [MeSH concept]
- neprilysin [MeSH Descriptor]
HGNC gene
- membrane metalloendopeptidase [HGNC gene]
NCIt concept(s)
- MME Gene [NCIt concept]
- MME wt Allele [NCIt concept]
- Neprilysin [NCIt concept]
ORDO concept(s)
- membrane metalloendopeptidase [ORDO Gene]
Phenotypes related
- Charcot-marie-tooth disease, axonal, type 2t [OMIM Phenotype]
- Spinocerebellar ataxia 43 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MME Gene [NCIt concept]
- membrane metalloendopeptidase [HGNC gene]

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