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intellectual disability, autosomal recessive 31 (MRT31) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

intellectual disability, autosomal recessive 31

MONDO:0013694

Also known as:MRT31mental retardation, autosomal recessive 31

Overview

GeneticsAutosomal recessive

ResearchLimited published research (6 articles)

Clinical Presentation

Features include: Intellectual disability.

Organ System	Phenotype Count	Example Features
Brain and nerves	1	Intellectual disability

Explore clinical features

Diagnosis

Biomarker and diagnostic research for intellectual disability, autosomal recessive 31 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 intellectual disability, autosomal recessive 31.

6 publications have been identified in PubMed for intellectual disability, autosomal recessive 31. Research spans Review / Meta-Analysis (33%), Case Report / Case Series (33%), and Diagnostic / Biomarker (17%).

Recent Publications

Manti F (2026). [PMID: 41450729](https://pubmed.ncbi.nlm.nih.gov/41450729/). *Neurol Genet*. [Epidemiology / Natural History]
Pan X (2026). [PMID: 41764152](https://pubmed.ncbi.nlm.nih.gov/41764152/). *J Mol Med (Berl)*. [Diagnostic / Biomarker]
Humeedat M (2025). [PMID: 40760536](https://pubmed.ncbi.nlm.nih.gov/40760536/). *Medicine (Baltimore)*. [Case Report / Case Series]
Webb BD (2025). [PMID: 40662098](https://pubmed.ncbi.nlm.nih.gov/40662098/). *Genet Med Open*. [Review / Meta-Analysis]
Yacoubian V (2024). [PMID: 38741921](https://pubmed.ncbi.nlm.nih.gov/38741921/). *Arthroplast Today*. [Review / Meta-Analysis]

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 9:40 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:614329

GARD

Genetic and Rare Diseases Info Center

GARD:22553

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 31

Overview

Clinical Presentation

Explore clinical features

Diagnosis

Research Landscape

Recent Publications

Medical References

External Resources

OMIM

GARD

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Questions for Your Care Team

Questions for Your Care Team