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Spermatogenic Failure 19

Disease ID: disease_node_15233

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DbxrefMIM:617592
SubclassofDOID_0050737, DOID_0111910
Data SourceDOID
SynonymsSPGF19
Doid Labelspermatogenic failure 19
Doid DescriptionA spermatogenic failure that is characterized by autosomal recessive inheritance of sperm flagellar morphological abnormalities that has_material_basis_in mutation in the CFAP43 gene on chromosome 10q25.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_15233
Doid IdDOID_0070170
LabelSpermatogenic Failure 19