Details of Disease | DrugMAP

General Information of Disease (ID: DIS2WS89)

Disease Name	Diabetes mellitus, permanent neonatal 4
Synonyms	DIABETES MELLITUS, PERMANENT NEONATAL 4; PNDM4; diabetes mellitus, permanent neonatal 4
Disease Hierarchy	DIS5AEXS: Permanent neonatal diabetes mellitus DIS2WS89: Diabetes mellitus, permanent neonatal 4
Disease Identifiers	MONDO ID MONDO_0030089 UMLS CUI C5394307 OMIM ID 618858 MedGen ID 1711191

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
INS	TTZOPHG	Strong	Autosomal dominant	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
INS	OTZ85PDU	Strong	Autosomal dominant	[1]
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References

1	The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources. Genet Med. 2022 Aug;24(8):1732-1742. doi: 10.1016/j.gim.2022.04.017. Epub 2022 May 4.