Peptidylglycine alpha-amidating monooxygenase

Preferred Label : Peptidylglycine alpha-amidating monooxygenase;

Symbol : PAM;

CISMeF acronym : PAM;

Type : Gene;

Ensembl ID : ENSG00000145730;

Prefixed ID : *170270;

Details

Origin ID

170270;

UMLS CUI

C1456357;

Automatic exact mappings (from CISMeF team)
- Conjunctival Melanocytic Intraepithelial Neoplasia [NCIt concept]
- MYC binding protein 2 [HGNC gene]
- MYCBP2 wt Allele [NCIt concept]
- Microscopic polyangiitis [ORDO Disease]
- Pampanga Language [NCIt concept]
- Potassium Aggravated Myotonia [NCIt concept]
- Potassium-aggravated myotonia [ORDO Disease]
- microscopic polyangiitis [MeSH Descriptor]
- peptidylglycine alpha-amidating monooxygenase [HGNC gene]
- peptidylglycine monooxygenase [MeSH Supplementary Concept]
HGNC gene
- peptidylglycine alpha-amidating monooxygenase [HGNC gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- peptidylglycine alpha-amidating monooxygenase [HGNC gene]

Keyword's position in hierarchy(ies) :

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