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intellectual disability, X-linked 88 (MRX88) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

intellectual disability, X-linked 88

MONDO:0010454

Also known as:MRX88intellectual disability, XMEN-linked 88mental retardation, X-linked 88

Overview

GeneticsX-linked

Clinical Presentation

Features include common findings: Seizure; and sometimes findings: Autism. 4 total HPO annotations.

Organ System	Phenotype Count	Example Features
Brain and nerves	3	Seizure, Global developmental delay, Intellectual disability

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Diagnosis

Biomarker and diagnostic research for intellectual disability, X-linked 88 has been reported in the published literature.

Prognosis

Phenotype severity distribution: 1 common feature.

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 88.

105 publications have been identified in PubMed for intellectual disability, X-linked 88. Kisho has analyzed 26 by research type. Research spans Epidemiology / Natural History (46%), Review / Meta-Analysis (23%), and Clinical Trial Publication (12%).

Research Type	Count	% of Total
Disease patterns and progression	12	46%

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 6:15 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:300852

GARD

Genetic and Rare Diseases Info Center

GARD:22692

Questions for Your Care Team

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intellectual disability, X-linked 88

Overview

Clinical Presentation

Explore clinical features

Diagnosis

Prognosis

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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