Global Variome shared LOVD

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

Phenotype #0000233292 Individual ID 00307866 Associated disease CLN2 Phenotype details Visual impairment, Delayed speech and language development, Seizures, Developmental regression Visual impairment, Delayed speech and language development, Seizures, Developmental regression Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis 01y11m Age/Onset - Phenotype/Onset - Protein - Owner name Corina-Marcela Rus Database submission license No license selected Created by Corina-Marcela Rus Date created 2020-08-20 00:41:10 +02:00 (CEST) Date last edited 2020-08-23 15:29:26 +02:00 (CEST)

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