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DOID:0080739 - Ehlers-Danlos syndrome spondylodysplastic type 3
Disease Ontology Definition:An Ehlers-Danlos syndrome that has_material_basis_in homozygous mutation in the zinc transporter gene SLC39A13 on chromosome 11p11 and that is characterized by short stature, hyperelastic skin and hypermobile joints, protuberant eyes with bluish sclerae, finely wrinkled palms, and characteristic radiologic features.
Synonyms:
Echinobase Genes
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| MIM:612350 - spondylocheirodysplasia, ehlers-danlos syndrome-like |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Ehlers-Danlos syndrome (is_a)