Global Variome shared LOVD

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Phenotype #0000215959 Individual ID 00281378 Associated disease TSC Diagnosis/Initial definite tuberous sclerosis TSC/Features - Diagnosis/Definite TSC-2 Inheritance Familial, autosomal dominant Phenotype details Cortical dysplasias,astrocytoma; Seizures; macules hypomelanotic. Mother has Angiofibroma, Hypomelanotic macules Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Seizures - Intellectual_dis - Protein - Cognitive/Impairment - Development - Owner name Rosemary Ekong Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Rosemary Ekong Date created 2017-12-12 12:50:47 +01:00 (CET) Date last edited 2018-08-28 15:30:57 +02:00 (CEST)

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