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Metadata
ID	DOID:0070568
Name	spermatogenic failure 69
Definition	A spermatogenic failure characterized by partial globozoospermia that has_material_basis_in homozygous mutation in the GGN on chromosome 19q13.2. https://pubmed.ncbi.nlm.nih.gov/33108537/, https://pubmed.ncbi.nlm.nih.gov/31985809/
Xrefs	MIM:619826
SKOS	exactMatch MIM:619826
Synonyms	SPGF69 [EXACT]
Parent Relationships	is_a spermatogenic failure is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance