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Metadata
ID	DOID:0112176
Name	spermatogenic failure 48
Definition	A spermatogenic failure that is characterized by impaired spermatogenesis, primarily occurring at meiosis that has_material_basis_in homozygous or compound heterozygous mutation in M1AP on chromosome 2p13.1. https://pubmed.ncbi.nlm.nih.gov/32017041/, https://pubmed.ncbi.nlm.nih.gov/32673564/
Xrefs	MIM:619108
Synonyms	SPGF48 [EXACT]
Parent Relationships	is_a spermatogenic failure is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance