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 11 - 20 of 29 in total
Gene ID Gene Symbol Description Source
4051 CYP4F3 cytochrome P450 family 4 subfamily F member 3
4099 MAG myelin associated glycoprotein
4534 MTM1 myotubularin 1
5230 PGK1 phosphoglycerate kinase 1
5236 PGM1 phosphoglucomutase 1
5332 PLCB4 phospholipase C beta 4
5621 PRNP prion protein (Kanno blood group)
5631 PRPS1 phosphoribosyl pyrophosphate synthetase 1
5743 PTGS2 prostaglandin-endoperoxide synthase 2
8898 MTMR2 myotubularin related protein 2
The Human Phenotype Ontology
Displaying entries 21 - 30 of 32 in total
HPO ID HPO Term
HP:0002522 Areflexia of lower limbs
HP:0000407 Sensorineural hearing impairment
HP:0003383 Onion bulb formation
HP:0001270 Motor delay
HP:0011463 Childhood onset
HP:0002460 Distal muscle weakness
HP:0000510 Rod-cone dystrophy
HP:0003481 Segmental peripheral demyelination/remyelination
HP:0001271 Polyneuropathy
HP:0003828 Variable expressivity
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