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Metadata
ID	DOID:0080733
Name	Ehlers-Danlos syndrome dermatosparaxis type
Definition	An Ehlers-Danlos syndrome that is characterized by severe skin fragility, sagging, redundant skin and that has_material_basis_in mutation in the gene encoding the procollagen protease ADAMTS2 on chromosome 5q35. https://pubmed.ncbi.nlm.nih.gov/28306229/
Xrefs	MIM:225410
Parent Relationships	is_a Ehlers-Danlos syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance