C9orf72 protein, human

Preferred Label : C9orf72 protein, human;

MeSH note : mutation leads to both chromsome 9p21-linked amyotrophic lateral sclerosis and frontotemporal dementia; GenBank BC020851;

MeSH synonym : chromosome 9 open reading frame 72 protein, human; MGC23980 protein, human;

Is substance : O;

Détails

Origin ID

C568651;

UMLS CUI

C3252868;

MeSH term(s) associated for indexing
- C9orf72 Protein [MeSH Descriptor]
- proteins [MeSH Descriptor]
Record concept(s)
- C9orf72 protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]
UMLS correspondences (same concept)
- Guanine Nucleotide Exchange Factor C9orf72 [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients