General Information of Disease (ID: DISBBWU2)

Disease Name Spermatogenic failure 65
Synonyms SPGF65
Disease Hierarchy
DIS3D1AI: Spermatogenic failure
DISBBWU2: Spermatogenic failure 65
Disease Identifiers
MONDO ID
MONDO_0030531
UMLS CUI
C5562067
OMIM ID
619712
MedGen ID
1794277

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
DNHD1 OT4U3HUW Strong Autosomal recessive [1]
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References

1 Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice. Am J Hum Genet. 2022 Jan 6;109(1):157-171. doi: 10.1016/j.ajhg.2021.11.022. Epub 2021 Dec 20.