Details of Disease | DrugMAP

General Information of Disease (ID: DISA30ZU)

Disease Name	Proteinuria, chronic benign
Synonyms	PROCHOB; PROTEINURIA, CHRONIC BENIGN; proteinuria, chronic benign
Disease Hierarchy	DISYKSRF: Genetic disease DISA30ZU: Proteinuria, chronic benign
Disease Identifiers	MONDO ID MONDO_0030042 UMLS CUI C5394384 OMIM ID 618884 MedGen ID 1714078

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
CUBN	TT9YLCR	Strong	Autosomal recessive	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
CUBN	OT5A9HD3	Strong	Autosomal recessive	[1]
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References

1	Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function. J Clin Invest. 2020 Jan 2;130(1):335-344. doi: 10.1172/JCI129937.