Phenotype #0000203793

Individual ID 00266013
Associated disease TSC
Diagnosis/Initial tuberous sclerosis
TSC/Features cysts renal;epilepsy
Diagnosis/Definite TSC-2
Inheritance Isolated (sporadic)
Phenotype details TSC2-PKD1 contiguous gene deletion syndrome
Age/Examination -
Age/Diagnosis 3y6m
Age/Onset -
Phenotype/Onset -
Seizures seizures
Intellectual_dis moderate
Protein -
Cognitive/Impairment -
Development -
Owner name Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2019-10-12 13:59:45 +02:00 (CEST)
Date last edited N/A

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