Details of Disease

General Information of Disease (ID: DISKG4GG)

Disease Name Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia
Disease Hierarchy
DIS372XH: Neurodevelopmental disorder
DISKG4GG: Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia
Disease Identifiers
MONDO ID
MONDO_0859137
UMLS CUI
C5543306
OMIM ID
619286
MedGen ID
1781371

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
MED27 OT40PZ9R Strong Autosomal recessive [1]
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References

1 Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen). Genet Med. 2020 Feb;22(2):245-257. doi: 10.1038/s41436-019-0686-8. Epub 2019 Nov 6.