Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/608380 http://purl.bioontology.org/ontology/OMIM/608380
Preferred Name	RETINITIS PIGMENTOSA 26
Synonyms	RP26
Type	http://www.w3.org/2002/07/owl#Class

altLabel	RP26
prefLabel	RETINITIS PIGMENTOSA 26
Gene Symbol	RP26 CERKL
Scope Statement	Onset by 15-20 years [MISCELLANEOUS] Caused by mutation in ceramide kinase-like gene (CERKL, 608381.0001) [MOLECULAR BASIS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU055673 http://purl.bioontology.org/ontology/OMIM/MTHU036671 http://purl.bioontology.org/ontology/OMIM/MTHU073695 http://purl.bioontology.org/ontology/OMIM/MTHU003279 http://purl.bioontology.org/ontology/OMIM/MTHU073693 http://purl.bioontology.org/ontology/OMIM/MTHU000322 http://purl.bioontology.org/ontology/OMIM/MTHU073694 http://purl.bioontology.org/ontology/OMIM/MTHU030342 http://purl.bioontology.org/ontology/OMIM/MTHU048966 See more See less
tui	T047
Gene Locus	2q31.3
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	608380
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000016
cui	C1842127
OMIM Entry Type	3
OMIM MimType Value	pound

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