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DOID:0080729 - brittle cornea syndrome 2
Disease Ontology Definition:An Ehlers-Danlos syndrome that has_material_basis_in homozygous mutation in the PRDM5 gene on chromosome 4q27.
Synonyms:
Xenbase Genes :
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Ehlers-Danlos syndrome (is_a),
autosomal recessive disease (is_a),
corneal disease (is_a)