Short stature homeobox

Preferred Label : Short stature homeobox;

Symbol : SHOX;

CISMeF acronym : SHOX;

Type : Gene;

Alternative titles and symbols : Pseudoautosomal homeobox-containing osteogenic gene; PHOG;

Ensembl ID : ENSG00000185960;

Prefixed ID : *312865;

Details

Origin ID

312865;

UMLS CUI

C1420041;

Automatic exact mappings (from CISMeF team)
- SHOX Gene [NCIt concept]
- SHOX gene [LOINC component]
- SHOX homeobox [HGNC gene]
- short stature homeobox [ORDO Gene]
HGNC gene
- SHOX homeobox [HGNC gene]
ORDO concept(s)
- short stature homeobox [ORDO Gene]
Phenotypes related
- Langer mesomelic dysplasia [OMIM Phenotype]
- Leri-weill dyschondrosteosis [OMIM Phenotype]
- Short stature, idiopathic, X-linked [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SHOX Gene [NCIt concept]
- SHOX gene [LOINC component]
- SHOX homeobox [HGNC gene]

Keyword's position in hierarchy(ies) :

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