Details of Disease | DrugMAP

General Information of Disease (ID: DIS8XEXM)

Disease Name	Porokeratosis 7, multiple types
Synonyms	POROK7; porokeratosis 7, multiple types; porokeratosis 7, disseminated superficial actinic type
Disease Hierarchy	DISELZ77: Disseminated superficial actinic porokeratosis DIS8XEXM: Porokeratosis 7, multiple types
Disease Identifiers	MONDO ID MONDO_0013868 UMLS CUI C3553549 OMIM ID 614714 MedGen ID 766463

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
MVD	TTE5J6X	Strong	Biomarker	[1]
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This Disease Is Related to 1 DME Molecule(s)

Gene Name	DME ID	Evidence Level	Mode of Inheritance	REF
MVD	DE7G63U	Strong	Autosomal dominant	[2]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
MVD	OTGEX4SR	Strong	Autosomal dominant	[2]
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References

1	[Analysis of clinical and genetic features of nine patients with disseminated superfacial actinic porokeratosis].Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Aug 10;34(4):481-485. doi: 10.3760/cma.j.issn.1003-9406.2017.04.003.
2	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.