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Spermatogenic Failure 13

Disease ID: disease_node_15221

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DbxrefMIM:615841
SubclassofDOID_0050737, DOID_0111910
Data SourceDOID
SynonymsSPGF13
Doid Labelspermatogenic failure 13
Doid DescriptionA spermatogenic failure that is characterized by autosomal recessive inheritance of azoospermia or oligozoospermia that has_material_basis_in mutation in the TAF4B gene on chromosome 18q11.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_15221
Doid IdDOID_0070182
LabelSpermatogenic Failure 13