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partial deletion of the long arm of chromosome 13 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

partial deletion of the long arm of chromosome 13

MONDO:0016911

Also known as:partial deletion of chromosome 13qpartial deletion of the long arm of chromosome type 13partial monosomy of chromosome 13q

Overview

A cytogenetic abnormality that refers to the allelic loss of all or part of the long arm of chromosome 13.

OnsetCONGENITAL

Diagnosis

Biomarker and diagnostic research for partial deletion of the long arm of chromosome 13 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 partial deletion of the long arm of chromosome 13.

16 publications have been identified in PubMed for partial deletion of the long arm of chromosome 13. Research spans Case Report / Case Series (31%), Basic Science / Preclinical (25%), and Epidemiology / Natural History (19%).

Research Type	Count	% of Total
Patient case studies	5	31%

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 9:36 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:262101

GARD

Genetic and Rare Diseases Info Center

GARD:20832

Questions for Your Care Team

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partial deletion of the long arm of chromosome 13

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications