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Metadata
ID	DOID:0112270
Name	spermatogenic failure 52
Definition	A spermatogenic failure that is characterized by non-obstructive azoospermia resulting from meiotic arrest at the spermatocyte stage that has_material_basis_in homozygous or compound heterozygous mutation in C14orf39 on chromosome 14q23.1. https://pubmed.ncbi.nlm.nih.gov/33508233/
Xrefs	MIM:619202
Synonyms	SPGF52 [EXACT]
Parent Relationships	is_a spermatogenic failure is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance