General Information of Disease (ID: DISQ2AM2)

Disease Name Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia
Synonyms ALS26
Disease Hierarchy
DISWZ9CJ: Familial amyotrophic lateral sclerosis
DISQ2AM2: Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia
Disease Identifiers
MONDO ID
MONDO_0030885
UMLS CUI
C5436882
OMIM ID
619133
MedGen ID
1771903

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
TIA1 OTGPN3P8 Limited Autosomal dominant [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.