Details of Disease | DrugMAP

General Information of Disease (ID: DIS4EI1H)

Disease Name	Spermatogenic failure 37
Synonyms	SPGF37; SPERMATOGENIC FAILURE 37
Disease Hierarchy	DIS3D1AI: Spermatogenic failure DIS4EI1H: Spermatogenic failure 37
Disease Identifiers	MONDO ID MONDO_0032744 UMLS CUI C5193091 OMIM ID 618429 MedGen ID 1677534

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
TTC21A	OTBJ9JKF	Strong	Autosomal recessive	[1]
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References

1	Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice. Am J Hum Genet. 2019 Apr 4;104(4):738-748. doi: 10.1016/j.ajhg.2019.02.020. Epub 2019 Mar 28.