Global Variome shared LOVD

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

Phenotype #0000310060 Individual ID 00418764 Associated disease neuropathy, optic Phenotype details Color vision defect (HP:0000551); Abnormality of visual evoked potentials (HP:0000649); Abnormal electroretinogram (HP:0000512) Diagnosis/Initial - Diagnosis/Definite - Inheritance Familial, autosomal dominant Age/Examination 51y (51 years) Age/Diagnosis - Age/Onset ? Phenotype/Onset - Protein - Owner name Mohamed Selhane Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Created by Mohamed Selhane Date created 2022-10-06 11:21:03 +02:00 (CEST) Date last edited 2024-03-17 12:16:44 +01:00 (CET)

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