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Spermatogenic Failure 20

Disease ID: disease_node_15216

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DbxrefMIM:617593
SubclassofDOID_0050737, DOID_0111910
Data SourceDOID
SynonymsSPGF20
Doid Labelspermatogenic failure 20
Doid DescriptionA spermatogenic failure that is characterized by autosomal recessive inheritance of sperm flagellar morphological abnormalities that has_material_basis_in mutation in the CFAP44 gene on chromosome 3q13.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_15216
Doid IdDOID_0070166
LabelSpermatogenic Failure 20