Visualize Submit Comment

Metadata
ID	DOID:0111914
Name	spermatogenic failure 35
Definition	A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in severely impaired sperm motility and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the QRICH2 gene on chromosome 17q25.1. https://pubmed.ncbi.nlm.nih.gov/30683861/
Xrefs	MIM:618341
Synonyms	SPGF35 [EXACT]
Parent Relationships	is_a spermatogenic failure is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance