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DO Term : trichorhinophalangeal syndrome type II [DOID:4998] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A syndrome that has_material_basis_in mutation of the EXT1 and TRPS1 gene which results_in multiple exostosis along with short stature and cone-shaped ends located_in epiphysis. The disease has_symptom sparse scalp hair, has_symptom thin upper lip, has_symptom rounded nose.
  • synonyms:
  • Trichorhinophalangeal dysplasia type II,
  • trichorhinophalangeal syndrome type 2,
  • MESH:D015826,
  • SNOMEDCT_US_2023_03_01:41069008,
  • 150230,
  • UMLS_CUI:C0023003,
  • ORDO:502,
  • NCI:C75118,
  • Langer-Giedion syndrome,
  • GARD:7801,
  • OMIM:150230
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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