intellectual disability, autosomal recessive 3

Rare Disease

MONDO:0012037

Also known as:

CC2D1A autosomal recessive non-syndromic intellectual disabilityMRT3autosomal recessive non-syndromic intellectual disability caused by mutation in CC2D1A

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the CC2D1A gene.

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