Details of Disease | DrugMAP

General Information of Disease (ID: DIS96VS8)

Disease Name	Nephronophthisis-like nephropathy 2
Disease Hierarchy	DISXU4HY: Nephronophthisis DIS96VS8: Nephronophthisis-like nephropathy 2
Disease Identifiers	MONDO ID MONDO_0859175 UMLS CUI C5561953 OMIM ID 619468 MedGen ID 1794163

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTP Molecule(s)

Gene Name	DTP ID	Evidence Level	Mode of Inheritance	REF
SLC41A1	DTB37ZE	Limited	Unknown	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
SLC41A1	OT4QBRK3	Limited	Unknown	[1]
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References

1	Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotype. J Am Soc Nephrol. 2013 May;24(6):967-77. doi: 10.1681/ASN.2012101034. Epub 2013 May 9.