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intellectual disability, autosomal recessive 11 (MRT11) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

intellectual disability, autosomal recessive 11

MONDO:0012619

Also known as:MRT11mental retardation, autosomal recessive, 11mental retardation, autosomal recessive 11

Overview

GeneticsAutosomal recessive

Clinical Presentation

Features include: Moderate intellectual disability.

Organ System	Phenotype Count	Example Features
Brain and nerves	1	Moderate intellectual disability

Explore clinical features

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 intellectual disability, autosomal recessive 11.

30 publications have been identified in PubMed for intellectual disability, autosomal recessive 11. Research spans Case Report / Case Series (52%), Review / Meta-Analysis (28%), and Epidemiology / Natural History (12%).

Research Type	Count	% of Total
Patient case studies	13	52%

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 11:56 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:611097

GARD

Genetic and Rare Diseases Info Center

GARD:22546

Questions for Your Care Team

→Should my partner and I meet with a genetic counselor to discuss carrier status and family planning?
→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

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intellectual disability, autosomal recessive 11

Overview

Clinical Presentation

Explore clinical features

Research Landscape

Medical References

External Resources

OMIM

GARD

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Questions for Your Care Team

Questions for Your Care Team

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