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Standards Ontologies Notations
retinitis pigmentosa 59

Summary
Synonym
  • RP59
Definition
A retinitis pigmentosa that has_material_basis_in mutation in the DHDDS gene on chromosome 1p36.11.
Super Class
autosomal recessive disease retinitis pigmentosa
Disease Ontology
DOID:0110352
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
79947 DHDDS dehydrodolichyl diphosphate synthase subunit
The Human Phenotype Ontology
Displaying entries 21 - 30 of 45 in total
HPO ID HPO Term
HP:0001513 Obesity
HP:0008046 Abnormal retinal vascular morphology
HP:0007737 Bone spicule pigmentation of the retina
HP:0001347 Hyperreflexia
HP:0007787 Posterior subcapsular cataract
HP:0005978 Type II diabetes mellitus
HP:0007994 Peripheral visual field loss
HP:0007703 Abnormality of retinal pigmentation
HP:0000007 Autosomal recessive inheritance
HP:0001250 Seizure
Displaying all 7 entries
Gene ID Gene Symbol Description
138050 HGSNAT heparan-alpha-glucosaminide N-acetyltransferase
3420 IDH3B isocitrate dehydrogenase (NAD(+)) 3 non-catalytic subunit beta
3419 IDH3A isocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha
5158 PDE6B phosphodiesterase 6B
55624 POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
762 CA4 carbonic anhydrase 4
79947 DHDDS dehydrodolichyl diphosphate synthase subunit
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024