General Information of Disease (ID: DIS4MZ8C)

Disease Name Usmani-Riazuddin syndrome, autosomal dominant
Disease Hierarchy
DISYKSRF: Genetic disease
DIS4MZ8C: Usmani-Riazuddin syndrome, autosomal dominant
Disease Identifiers
MONDO ID
MONDO_0859174
UMLS CUI
C5561952
OMIM ID
619467
MedGen ID
1794162

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
AP1G1 OTEO6Y9H Strong Autosomal dominant [1]
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References

1 De novo and bi-allelic variants in AP1G1 cause neurodevelopmental disorder with developmental delay, intellectual disability, and epilepsy. Am J Hum Genet. 2021 Jul 1;108(7):1330-1341. doi: 10.1016/j.ajhg.2021.05.007. Epub 2021 Jun 7.