Phenotype #0000000829

Individual ID 00001675
Associated disease KTZS
Phenotype details normal development until seizure onset,psychomotor regression after age 18 months, severe intellectual disability; admin;; amelogenesis imperfecta, hypoplastic rough teeth, yellow teeth
Diagnosis/Initial -
Inheritance Familial
Diagnosis/Definite -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Age/Examination -
Protein -
Owner name Division of Human Genetics, Innsbruck
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Division of Human Genetics, Innsbruck
Date created 2012-10-23 11:53:21 +02:00 (CEST)
Date last edited 2020-11-27 17:43:21 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.