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Metadata
ID	DOID:0080739
Name	Ehlers-Danlos syndrome spondylodysplastic type 3
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. https://pubmed.ncbi.nlm.nih.gov/18513683/
Xrefs	OMIM:612350
Parent Relationships	is_a Ehlers-Danlos syndrome