syndromic X-linked intellectual disability Claes-Jensen type

Summary
Synonym
  • MRXSCJ
  • MRXSJ
  • mental retardation, X-linked, syndromic, Claes-Jensen type
  • syndromic X-linked intellectual disability due to JARID1C mutation
  • syndromic X-linked mental retardation JARID1C-related
Definition
A syndromic X-linked intellectual disability characterized by severe intellectual deficit associated with variable clinical manifestations including spasticity, cryptorchidism, maxillary hypoplasia, alopecia areata, epilepsy, short stature, impaired speech and behavioral problems that has_material_basis_in mutation in the KDM5C gene on chromosome Xp11.
Super Class
X-linked recessive disease syndromic X-linked intellectual disability
Disease Ontology
DOID:0060809
Mondo Disease Ontology
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
10765 KDM5B lysine demethylase 5B

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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