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Spermatogenic Failure 21

Disease ID: disease_node_15159

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DbxrefMIM:617644
SubclassofDOID_0050737, DOID_0112311
Data SourceDOID
Doid Labelspermatogenic failure 21
Doid DescriptionA male infertility due to acephalic spermatozoa that is characterized by acephalic spermatozoa, reduced sperm number and impaired sperm motility that has_material_basis_in homozygous mutation in the BRDT gene on chromosome 1p22.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_15159
Doid IdDOID_0070163
LabelSpermatogenic Failure 21