Details of Disease

General Information of Disease (ID: DIS6VVNV)

Disease Name Spermatogenic failure 69
Synonyms SPGF69; spermatogenic failure 69
Disease Hierarchy
DIS3D1AI: Spermatogenic failure
DIS6VVNV: Spermatogenic failure 69
Disease Identifiers
MONDO ID
MONDO_0030732
UMLS CUI
C5676960
OMIM ID
619826
MedGen ID
1811285

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
GGN OTKPYNWP Limited Autosomal recessive [1]
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References

1 Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia. Hum Reprod. 2020 Jan 1;35(1):240-252. doi: 10.1093/humrep/dez246.