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renal caliceal diverticuli-deafness syndrome - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

renal caliceal diverticuli-deafness syndrome

MONDO:0017281

Overview

Clinical Presentation

Built from Human Phenotype Ontology (HPO) phenotype annotations and GeneReviews clinical descriptions. Features represent findings documented across known cases — not an exhaustive list of possible symptoms.

Features include very common findings: Abnormality of the kidney, Abnormality of the urinary system, and Inner ear hearing loss (sensorineural hearing impairment); and sometimes findings: Hydroureter, Hydronephrosis, and Abnormality of the upper urinary tract.

Organ System	Phenotype Count	Example Features
Kidneys and urinary system	3	Abnormality of the kidney, Abnormality of the urinary system, Abnormality of the upper urinary tract
Ears

Prognosis

Phenotype severity distribution: 3 very common features.

Estimated prevalence: <1 in 1,000,000 (VERY_RARE).

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 9:42 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:2838

GARD

Genetic and Rare Diseases Info Center

GARD:4655

Questions for Your Care Team

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renal caliceal diverticuli-deafness syndrome

Overview

Clinical Presentation

Prognosis

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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