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Metadata
ID	DOID:0111921
Name	spermatogenic failure 36
Definition	A spermatogenic failure characterized by spermatozoa showing anomalies of the head, acrosome, and nucleus of the sperm resulting in reduced fertility that has_material_basis_in heterozygous mutation in the PPP2R3C gene on chromosome 14q13.2. https://pubmed.ncbi.nlm.nih.gov/30893644/
Xrefs	MIM:618420
Synonyms	SPGF36 [EXACT]
Parent Relationships	is_a autosomal dominant disease is_a spermatogenic failure
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance