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autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome

MeSH: C567088ORPHA: 73229

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

medical condition

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Clinical Presentation

Signs and symptoms associated with autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome, sourced from HPO and Orphanet clinical annotations.

Renal insufficiencyMuscle spasmMultiple renal cystsRetinal vascular tortuosityHematuria

Classification & Codes

MeSH Code

C567088

Orphanet Code

ORPHA:73229
autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome
MeSHC567088
OrphanetORPHA:73229
Treatments0 drug(s)
Symptoms on record5 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO