Details of Disease | DrugMAP

General Information of Disease (ID: DIS8MZMJ)

Disease Name	Retinitis pigmentosa 89
Synonyms	RETINITIS PIGMENTOSA 89; RP89; retinitis pigmentosa 89
Disease Hierarchy	DISYKSRF: Genetic disease DIS8MZMJ: Retinitis pigmentosa 89
Disease Identifiers	MONDO ID MONDO_0030071 UMLS CUI C5394552 OMIM ID 618955 MedGen ID 1710499

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
KIF3B	OT0HJREB	Strong	Autosomal dominant	[1]
------------------------------------------------------------------------------------

References

1	Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy. Am J Hum Genet. 2020 Jun 4;106(6):893-904. doi: 10.1016/j.ajhg.2020.04.005. Epub 2020 May 7.