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autosomal recessive non-syndromic intellectual disability - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal recessive non-syndromic intellectual disability

MONDO:0019502

Also known as:autosomal recessive intellectual disabilityintellectual disability, autosomal recessiveAR-NSID

Overview

Autosomal recessive form of non-syndromic intellectual disability.

OnsetINFANTILE, CONGENITAL, JUVENILE, LATE, CHILDHOOD, NEONATAL

Diagnosis

Biomarker and diagnostic research for autosomal recessive non-syndromic intellectual disability has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for autosomal recessive non-syndromic intellectual disability.

110 publications have been identified in PubMed for autosomal recessive non-syndromic intellectual disability. Kisho has analyzed 24 by research type. Research spans Basic Science / Preclinical (42%), Case Report / Case Series (33%), and Review / Meta-Analysis (13%).

Research Type	Count	% of Total
Laboratory research	10	42%

Data assembled from 3 of 12 sources · Last updated Oct 3, 2026, 5:10 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:88616

GARD

Genetic and Rare Diseases Info Center

GARD:18643

Questions for Your Care Team

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autosomal recessive non-syndromic intellectual disability

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications