Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000129987 Individual ID 00163021 Associated disease AHC1 Phenotype details Epilepsy, Abnormal eye movement, Dystonia, automatic dysfunction, and slight developmental delay. Diagnosis/Initial AHC Inheritance Familial, autosomal dominant Diagnosis/Definite AHC Age/Examination 02y (2 years) Age/Diagnosis 02y Age/Onset 00y01m Phenotype/Onset seizure Protein - Owner name Xiaoxu Yang Database submission license No license selected Created by Xiaoxu Yang Date created 2018-06-24 19:48:07 +02:00 (CEST) Date last edited 2018-06-26 09:08:30 +02:00 (CEST)

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