/autism, susceptibility to, X-linked 2

autism, susceptibility to, X-linked 2

MONDO:0010341

Also Known As

AUTSX2autism susceptibility, X-linked 2, isolated cases, X-linkedautism, susceptibility to, X-linked 2autism, susceptibility to, X-linked type 2intellectual developmental disorder, X-linked, Isolated cases, X-linkedintellectual disability, X-linkedmental retardation, X-linkedsusceptibility to X-linked autism 2

Definition

A class of genetic disorders resulting in intellectual disability that is associated either with mutations of genes located on the X chromosome or aberrations in the structure of the X chromosome (sex chromosome aberrations).

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

NLGN4X ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:300495 ↗

Related Diseases

autism, susceptibility to, X-linked 1

MONDO:0010321

autism, susceptibility to, X-linked 3

MONDO:0010342

autism, susceptibility to, X-linked 4

MONDO:0010440

autism, susceptibility to, X-linked 5

MONDO:0010449

epsilon-trimethyllysine hydroxylase deficiency

MONDO:0010469

intellectual developmental disorder with autism and speech delay

MONDO:0011627

← Back to All Diseases