Global Variome shared LOVD

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

Phenotype #0000339018 Individual ID 00449871 Associated disease SCZD Phenotype details Schizophrenia, Scoliosis, Aplasia/Hypoplasia of the cerebellar vermis, Neurodevelopmental delay Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Camille Verebi Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Created by Camille Verebi Date created 2024-05-21 16:57:29 +02:00 (CEST) Date last edited 2024-05-22 09:36:38 +02:00 (CEST)

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