ENAM protein, human

Preferred Label : ENAM protein, human;

MeSH note : mutation leads to local hypoplastic form of autosomal dominant amelogenesis imperfecta; GenBank AF125373;

MeSH synonym : enamelin protein, human; AIH2 protein, human; amelogenesis imperfecta 2, hypocalcification (autosomal dominant) protein, human;

Is substance : O;

Details

Origin ID

C550525;

UMLS CUI

C2935053;

MeSH term(s) associated for indexing
- extracellular matrix proteins [MeSH Descriptor]
- proteins [MeSH Descriptor]
Record concept(s)
- ENAM protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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