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 21 - 29 of 29 in total
Gene ID Gene Symbol Description Source
9517 SPTLC2 serine palmitoyltransferase long chain base subunit 2
9896 FIG4 FIG4 phosphoinositide 5-phosphatase
10558 SPTLC1 serine palmitoyltransferase long chain base subunit 1
10855 HPSE heparanase
23175 LPIN1 lipin 1
23600 AMACR alpha-methylacyl-CoA racemase
27036 SIGLEC7 sialic acid binding Ig like lectin 7
51196 PLCE1 phospholipase C epsilon 1
84649 DGAT2 diacylglycerol O-acyltransferase 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