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X-Linked Congenital Bilateral Absence Of Vas Deferens

Disease ID: disease_node_17153

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DbxrefMIM:300985
SubclassofDOID_0111862
Data SourceDOID
SynonymsCBAVDX
Doid LabelX-linked congenital bilateral absence of vas deferens
Doid DescriptionA congenital bilateral absence of vas deferens that has_material_basis_in mutation in the ADGRG2 gene on chromosome Xp22.13.
Disease Node Iddisease_node_17153
Doid IdDOID_0111863
Disease Has Basis InHP_0001197
LabelX-Linked Congenital Bilateral Absence Of Vas Deferens