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DO Term : SHOX-related short stature [DOID:0112120] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A bone development disease characterized by height below the third percentile for chronological age that has_material_basis_in mutation in the SHOX gene or the SHOXY gene on chromosomes Xp22.33 and Yp11.2, respectively.
  • synonyms:
  • OMIM:300582,
  • idiopathic familial short stature,
  • 300582,
  • ORDO:314795
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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