Global Variome shared LOVD

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

Phenotype #0000002899 Individual ID 00001640 Associated disease FVH2 Phenotype details secondary nystagmus and low vision Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite FVH2 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Yonatan Perez Database submission license No license selected Created by Johan den Dunnen Date created 2013-12-24 22:34:45 +01:00 (CET) Date last edited 2022-01-19 20:06:57 +01:00 (CET)

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