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familial temporal lobe epilepsy 5

ORPHA: 163717

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Classification & Codes

Overview

temporal lobe epilepsy that has material basis in heterozygous mutation in the CPA6 gene on chromosome 8q13

Available Treatments (0)

No treatments linked yet

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

Classification & Codes

Orphanet Code

ORPHA:163717
familial temporal lobe epilepsy 5
OrphanetORPHA:163717
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
familial temporal lobe epilepsy 5 | OrphanDrug