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DO Term : Ehlers-Danlos syndrome dermatosparaxis type [DOID:0080733] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • OMIM:225410,
  • 225410
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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