Non-specific syndromic intellectual disability

Get in touch with RARE Concierge.

Contact RARE Concierge

Synonyms: Complex neurodevelopmental disorder

A rare genetic intellectual disability characterized by the association of intellectual disability with variable other anomalies in the absence of a well-characterized syndrome. Associated abnormalities may include facial dysmorphism neurological signs and symptoms behavioral problems and abnormalities of various other organ systems.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version June 2024

Newly diagnosed with
Non-specific syndromic intellectual disability?

Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.

Get Concierge Help

Advocacy Organizations

AGO2 Association

AGO Alliance is dedicated to improving the lives of children affected by Argonaute Syndromes (AGO1 & AGO2 genes) by accelerating the development of therapeutics, bringing families together, and providing education.

Project CASK

VISION Project CASK believes in a world free of the life limitations and debilitating effects of CASK gene disorders. ​MISSION To accelerate breakthroughs in research to develop treatments and a cure for CASK gene disorders. ​VALUES Collaboration. Transparency. Urgency.

Don't see your organization here. Let us know here.

Clinical Trials

For a list of clinical trials in this disease area, please click here.