Kisho

Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy

intellectual disability, X-linked 73 (MRX73) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

intellectual disability, X-linked 73

MONDO:0010307

Also known as:MRX73mental retardation, X-linked 73, X-linked recessivemental retardation, X-linked 73

Overview

GeneticsX-linked

Clinical Presentation

Features include: Mild intellectual disability and Synophrys.

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

Explore clinical features

Diagnosis

Biomarker and diagnostic research for intellectual disability, X-linked 73 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, X-linked 73.

30 publications have been identified in PubMed for intellectual disability, X-linked 73. Research spans Epidemiology / Natural History (23%), Diagnostic / Biomarker (20%), and Review / Meta-Analysis (20%).

Research Type	Count	% of Total
Disease patterns and progression	7	23%

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 6:44 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:300355

GARD

Genetic and Rare Diseases Info Center

GARD:22673

Questions for Your Care Team

→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

← Back to All Diseases

intellectual disability, X-linked 73

Overview

Clinical Presentation

Explore clinical features

Diagnosis

Research Landscape

Medical References

External Resources

OMIM

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications