|  Help  |  About  |  Contact Us

DO Term : spondyloepimetaphyseal dysplasia, Strudwick type [DOID:0080028] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spondyloepimetaphyseal dysplasia that has_material_basis_in mutations in the COL2A1 gene which results_in short stature and multiple skeletal abnormalities (lordosis, scoliosis, flattened vertebrae, pectus carinatum, coxa vara, clubfoot, and abnormal epiphyses or metaphyses).
  • synonyms:
  • OMIM:184250,
  • ORDO:93346,
  • 184250,
  • GARD:134
Quick Links:
 
Quick Links:
 

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