Aristaless-related homeobox, X-linked

Preferred Label : Aristaless-related homeobox, X-linked;

Symbol : ARX;

CISMeF acronym : ARX;

Type : Gene;

Ensembl ID : ENSG00000004848;

Prefixed ID : *300382;

Details

Origin ID

300382;

UMLS CUI

C1425272;

Automatic exact mappings (from CISMeF team)
- ARX Gene [NCIt concept]
- ARX gene [LOINC component]
- UBA2 wt Allele [NCIt concept]
- aristaless related homeobox [HGNC gene]
- aristaless related homeobox [ORDO Gene]
HGNC gene
- aristaless related homeobox [HGNC gene]
NCIt concept(s)
- ARX Gene [NCIt concept]
- ARX wt Allele [NCIt concept]
- Homeobox Protein ARX [NCIt concept]
ORDO concept(s)
- aristaless related homeobox [ORDO Gene]
Phenotypes related
- Corpus callosum, agenesis of, with abnormal genitalia [OMIM Phenotype]
- Developmental and epileptic encephalopathy 1 [OMIM Phenotype]
- Intellectual developmental disorder, X-linked 29 [OMIM Phenotype]
- Lissencephaly, X-linked, 2 [OMIM Phenotype]
- Partington syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ARX Gene [NCIt concept]
- ARX gene [LOINC component]
- aristaless related homeobox [HGNC gene]

Keyword's position in hierarchy(ies) :

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