Arts syndrome

Summary
Synonym
  • ARTS
  • Lethal ataxia with deafness and optic atrophy
  • MRXS18
  • MRXSARTS
  • fatal X-linked ataxia with deafness and loss of vision
  • syndromic X-linked mental retardation 18
  • syndromic X-linked mental retardation Arts type
Definition
An X-linked disease that is characterized by profound congenital sensorineural hearing impairment, early-onset hypotonia, delayed motor development, mild to moderate intellectual disability, ataxia, and increased risk of infection and has_material_basis_in mutations of the PRPS1 gene.
Super Class
syndromic X-linked intellectual disability
Disease Ontology
DOID:0050647
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
Related Genes
Displaying all 3 entries
Gene ID Gene Symbol Description Source
5308 PITX2 paired like homeodomain 2
5631 PRPS1 phosphoribosyl pyrophosphate synthetase 1
5635 PRPSAP1 phosphoribosyl pyrophosphate synthetase associated protein 1
Displaying all 2 entries
Gene ID Gene Symbol Description Source
19139 Prps1 phosphoribosyl pyrophosphate synthetase 1
67763 Prpsap1 phosphoribosyl pyrophosphate synthetase-associated protein 1
The Human Phenotype Ontology
Displaying entries 1 - 10 of 43 in total
HPO ID HPO Term
HP:0000467 Neck muscle weakness
HP:0000505 Visual impairment
HP:0000618 Blindness
HP:0000639 Nystagmus
HP:0000648 Optic atrophy
HP:0001251 Ataxia
HP:0001256 Intellectual disability, mild
HP:0001270 Motor delay
HP:0001284 Areflexia
HP:0001324 Muscle weakness
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: December 9, 2024