Details of Disease | DrugMAP

General Information of Disease (ID: DISLE1RM)

Disease Name	Spermatogenic failure 33
Synonyms	SPERMATOGENIC FAILURE 33; SPGF33
Disease Hierarchy	DIS3D1AI: Spermatogenic failure DISLE1RM: Spermatogenic failure 33
Disease Identifiers	MONDO ID MONDO_0029147 UMLS CUI C4748395 OMIM ID 618152 MedGen ID 1648473

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
CFAP251	OT0GKNAU	Strong	Autosomal recessive	[1]
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References

1	A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility. Am J Hum Genet. 2018 Sep 6;103(3):400-412. doi: 10.1016/j.ajhg.2018.07.014. Epub 2018 Aug 16.