Global Variome shared LOVD

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

Phenotype #0000296585 Individual ID 00403992 Associated disease OCMD Phenotype details Retinal dystrophy, Abnormality of metabolism/homeostasis, Somatic sensory dysfunction, Deep white matter hypodensities, Periventricular white matter hyperintensities, Optic neuritis Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - Age/Examination 09y (9 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2022-02-25 14:03:41 +01:00 (CET) Date last edited 2022-02-25 14:16:13 +01:00 (CET)

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