Methyl-cpg-binding protein 2

Preferred Label : Methyl-cpg-binding protein 2;

Symbol : MECP2;

CISMeF acronym : MECP2;

Type : Gene;

Ensembl ID : ENSG00000169057;

Prefixed ID : *300005;

Details

Origin ID

300005;

UMLS CUI

C1417098;

Automatic exact mappings (from CISMeF team)
- MECP2 Gene [NCIt concept]
- MECP2 gene [LOINC component]
- MECP2 wt Allele [NCIt concept]
- Methyl-CpG-Binding Protein 2 [NCIt concept]
- Methyl-CpG-Binding protein 2 [MeSH concept]
- methyl-CpG binding protein 2 [HGNC gene]
- methyl-CpG binding protein 2 [ORDO Gene]
- methyl-cpg-binding protein 2 [MeSH Descriptor]
HGNC gene
- methyl-CpG binding protein 2 [HGNC gene]
NCIt concept(s)
- MECP2 Gene [NCIt concept]
- MECP2 wt Allele [NCIt concept]
- Methyl-CpG-Binding Protein 2 [NCIt concept]
ORDO concept(s)
- methyl-CpG binding protein 2 [ORDO Gene]
Phenotypes related
- Autism, susceptibility to, X-linked 3 [OMIM Phenotype]
- Encephalopathy, neonatal severe, due to mecp2 mutations [OMIM Phenotype]
- Intellectual developmental disorder, X-linked, syndromic 13 [OMIM Phenotype]
- Intellectual developmental disorder, X-linked, syndromic, lubs type [OMIM Phenotype]
- Rett syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MECP2 Gene [NCIt concept]
- MECP2 gene [LOINC component]
- methyl-CpG binding protein 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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