Global Variome shared LOVD

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Phenotype #0000212699 Individual ID 00278118 Associated disease TSC Diagnosis/Initial tuberous sclerosis TSC/Features - Diagnosis/Definite TSC-2 Inheritance Familial, autosomal dominant Phenotype details affected parent has one nail groove and one hypomelanotic macule 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 2008-07-29 08:47:16 +02:00 (CEST) Date last edited 2013-03-22 15:44:19 +01:00 (CET)

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