Global Variome shared LOVD

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

Phenotype #0000292519 Individual ID 00399408 Associated disease FVH2 Phenotype details Hypoplasia of the fovea (HP:0007750), Nystagmus (HP:0000639) and Iris transillumination defect (HP:0012805) Diagnosis/Initial Albinism Inheritance Familial, autosomal recessive Diagnosis/Definite Foveal hypoplasia 2 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein rs1161159416 Owner name Mohammed A.M Derar Database submission license Creative Commons Attribution-NonCommercial 4.0 International Created by Mohammed A.M Derar Date created 2022-01-20 16:16:06 +01:00 (CET) Date last edited 2022-01-24 13:18:03 +01:00 (CET)

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