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autosomal recessive hypophosphatemic rickets (ARHR) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal recessive hypophosphatemic rickets

MONDO:0017324

Also known as:ARHRautosomal recessive hereditary hypophosphatemic ricketshereditary hypophosphatemic rickets, autosomal recessive

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Overview

Autosomal recessive hypophosphatemic rickets (ARHR) is a hereditary renal phosphate-wasting disorder characterized by hypophosphatemia, rickets and/or osteomalacia and slow growth.

Clinical Trials4 registered

Prognosis

Estimated prevalence: Unknown (Unknown prevalence).

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.

4 clinical trials registered. Interventions under study include drug therapy. Pipeline includes 2 PHASE3, 1 PHASE2, 1 PHASE1. Research is primarily industry-sponsored.

28 publications have been identified in PubMed for autosomal recessive hypophosphatemic rickets. Research spans Review / Meta-Analysis (29%), Case Report / Case Series (29%), and Epidemiology / Natural History (18%).

Research Type	Count	% of Total
Research summaries	8	29%

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 1:07 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:289176

GARD

Genetic and Rare Diseases Info Center

GARD:17320

Questions for Your Care Team

→Are any of the 4 active clinical trials a good fit for my situation?
→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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autosomal recessive hypophosphatemic rickets

Overview

Prognosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Subtypes

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Questions for Your Care Team

Questions for Your Care Team

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