Details of Disease

General Information of Disease (ID: DIS5ILXC)

Disease Name Nephronophthisis 20
Synonyms nephronophthisis 20; NPHP20; nephronophthisis (disease) caused by mutation in MAPKBP1; nephronophthisis type 20; MAPKBP1 nephronophthisis (disease)
Definition Any nephronophthisis in which the cause of the disease is a mutation in the MAPKBP1 gene.
Disease Hierarchy
DISXU4HY: Nephronophthisis
DIS5ILXC: Nephronophthisis 20
Disease Identifiers
MONDO ID
MONDO_0014997
UMLS CUI
C4310640
OMIM ID
617271
MedGen ID
934607

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
MAPKBP1 OTMLEJ67 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.