Charcot-Marie-Tooth disease X-linked recessive 5

Summary
Synonym
  • CMT5X
  • CMTX5
  • Charcot-Marie-Tooth neuropathy X-linked recessive 5
  • Rosenberg-Chutorian syndrome
  • X-linked Charcot-Marie-Tooth disease type 5
  • optic atrophy, polyneuropathy, and deafness
Definition
A Charcot-Marie-Tooth disease X-linked that has_material_basis_in loss-of-function mutation in the PRPS1 gene on chromosome Xq22.
Super Class
Charcot-Marie-Tooth disease type X X-linked recessive disease
External Links
Disease Ontology
DOID:0110210
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying entries 1 - 10 of 29 in total
Gene ID Gene Symbol Description Source
410 ARSA arylsulfatase A
821 CANX calnexin
847 CAT catalase
960 CD44 CD44 molecule (IN blood group)
1636 ACE angiotensin I converting enzyme
2629 GBA1 glucosylceramidase beta 1
2877 GPX2 glutathione peroxidase 2
3032 HADHB hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta
3098 HK1 hexokinase 1
3931 LCAT lecithin-cholesterol acyltransferase
The Human Phenotype Ontology
Displaying entries 11 - 20 of 32 in total
HPO ID HPO Term
HP:0001761 Pes cavus
HP:0000763 Sensory neuropathy
HP:0002808 Kyphosis
HP:0001284 Areflexia
HP:0007328 Impaired pain sensation
HP:0001324 Muscle weakness
HP:0001260 Dysarthria
HP:0002463 Language impairment
HP:0003693 Distal amyotrophy
HP:0000529 Progressive visual loss
Displaying 1 entry
Gene ID Gene Symbol Description
5631 PRPS1 phosphoribosyl pyrophosphate synthetase 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024