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Metadata
ID	DOID:0070598
Name	X-linked spermatogenic failure 7
Definition	A spermatogenic failure characterized by sperm with insufficient individualization, excessive residual cytoplasm, acrosome defects, and abnormalities of the head and flagella, resulting in significantly reduced sperm concentration and progressive motility, that has_material_basis_in hemizygous mutation in the CT55 gene on chromosome Xq26.3. https://pubmed.ncbi.nlm.nih.gov/36481789/
Xrefs	MIM:301106
SKOS	exactMatch MIM:301106
Synonyms	SPGFX7 [EXACT]
Parent Relationships	is_a spermatogenic failure is_a X-linked recessive disease
Subclass Logical Relationships	has material basis in some X-linked recessive inheritance