Global Variome shared LOVD

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

Phenotype #0000292476 Individual ID 00399365 Associated disease FVH2 Phenotype details foveal hypoplasia (HP:0007750), nystagmus (HP:0000639) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite FVH2 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2022-01-19 22:05:08 +01:00 (CET) Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.