Details of Disease | DrugMAP

General Information of Disease (ID: DISC7KWQ)

Disease Name	Spermatogenic failure 7
Synonyms	SPGF7; Male infertility, nonsyndromic, autosomal recessive; spermatogenic failure 7; spermatogenic failure type 7
Disease Hierarchy	DIS3D1AI: Spermatogenic failure DISC7KWQ: Spermatogenic failure 7
Disease Identifiers	MONDO ID MONDO_0013070 MESH ID C567832 UMLS CUI C2751811 OMIM ID 612997 MedGen ID 414478

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
CATSPER1	TT5CISB	Limited	Unknown	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
CATSPER1	OTPCTSQZ	Limited	Unknown	[1]
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References

1	Human male infertility caused by mutations in the CATSPER1 channel protein. Am J Hum Genet. 2009 Apr;84(4):505-10. doi: 10.1016/j.ajhg.2009.03.004. Epub 2009 Apr 2.