intellectual disability, autosomal recessive 61

Rare Disease

MONDO:0030915

Also known as:

intellectual disability, autosomal recessive 61Alwadei syndromeMRT61

An autosomal recessive non-syndromic intellectual disability that has material basis in an autosomal recessive mutation of the RUSC2 gene on chromosome 9p13.

Genes

Clinical Trials

–

Newborn Screening

–

Patient Groups

–

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

How we create this content →

Report Generation Failed

We couldn't automatically generate the report. This may be due to temporary service issues.

Need this data in your product?

Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.

Explore API Start Free

← Back to All Diseases

intellectual disability, autosomal recessive 61

Patient-Friendly Information

Need this data in your product?

Companies Active in intellectual disability, autosomal recessive 61