Details of Disease | DrugMAP

General Information of Disease (ID: DISLH7U4)

Disease Name	Spermatogenic failure 42
Synonyms	SPGF42; SPERMATOGENIC FAILURE 42
Disease Hierarchy	DIS3D1AI: Spermatogenic failure DISLH7U4: Spermatogenic failure 42
Disease Identifiers	MONDO ID MONDO_0032896 UMLS CUI C5231488 OMIM ID 618745 MedGen ID 1684744

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
TTC29	OT37KCUL	Strong	Autosomal recessive	[1]
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References

1	Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility. Am J Hum Genet. 2019 Dec 5;105(6):1148-1167. doi: 10.1016/j.ajhg.2019.10.007. Epub 2019 Nov 14.