Aldosterone-producing adenoma with seizures and neurological abnormalities: genes and variants

Aldosterone-producing adenoma with seizures and neurological abnormalities is linked to 1 analyzed protein (CACNA1D). 3 DNA variants are known to cause it; 44 more are uncertain, and 0 of those already look disease-causing on computable evidence.

Last updated 2026-09-30. Research information, not medical advice.

Genes linked to Aldosterone-producing adenoma with seizures and neurological abnormalities

Known disease-causing variants in Aldosterone-producing adenoma with seizures and neurological abnormalities

VariantPositionProtein partClinical label
CACNA1D G233D233IDisease-causing (★)
CACNA1D F747L747IIDisease-causing (★)
CACNA1D I750M750IIDisease-causing

Diseases related to Aldosterone-producing adenoma with seizures and neurological abnormalities

Frequently asked questions

Which genes are linked to Aldosterone-producing adenoma with seizures and neurological abnormalities?

In CATVariant, Aldosterone-producing adenoma with seizures and neurological abnormalities is linked to 1 analyzed protein: CACNA1D (Voltage-dependent L-type calcium channel subunit alpha-1D).

How many genetic variants are linked to Aldosterone-producing adenoma with seizures and neurological abnormalities?

51 variants: 3 are classified as disease-causing (pathogenic or likely pathogenic) in ClinVar and 44 are of uncertain significance or have conflicting reports.

Which uncertain variants in Aldosterone-producing adenoma with seizures and neurological abnormalities look disease-causing?

None of the uncertain variants currently reaches the likely-pathogenic range on computable evidence alone.

About this data

Variant–disease links come from ClinVar, Open Targets and UniProt, pooled from the latest public CATVariant analysis of each human protein. Evidence scores use the ACMG/AMP Bayesian points scale with computable criteria only (position among known disease variants, rarity in gnomAD, calibrated predictors, deep mutational scanning); there is no family or patient data, so they prioritise variants for expert review and never classify them.

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