Phenotype #0000142641
| Individual ID |
00180187 |
| Associated disease |
? |
| Diagnosis/Initial |
epilepsy or seizures associated with neurodevelopmental disorders and/or congenital malformations |
| Diagnosis/Definite |
Primary aldosteronism, seizures, and neurologic abnormalities |
| Phenotype details |
Epilepsy (HP:0001250), generalized tonic-clonic seizures (HP:0025190), left ventricular hypertrophy (HP:0001712), horseshoe kidney (HP:0000085), facial dysmorphism (HP:0001999), neuroblastoma (HP:0003006). |
| Inheritance |
Familial, autosomal dominant |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Tumor/MSI |
- |
| Diagnosis/Criteria |
- |
| Owner name |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2018-08-24 19:40:22 +02:00 (CEST) |
| Date last edited |
N/A |
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