Global Variome shared LOVD

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

Phenotype #0000274627 Individual ID 00380774 Associated disease CLN8 Inheritance Familial Diagnosis/Initial - Age/Examination - Diagnosis/Definite Ceroid lipofuscinosis type 8 Age/Diagnosis - Age/Onset - Phenotype/Onset - Phenotype details DD; ID; seizures; regression; cerebellar atrophy (Neurological) Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2021-08-23 12:15:23 +02:00 (CEST) Date last edited N/A

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