Global Variome shared LOVD

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

Phenotype #0000273611 Individual ID 00379757 Associated disease albinism Diagnosis/Initial albinism, ocular Diagnosis/Definite - Phenotype details Severely reduced visual acuity (HP:0001141); Nyctalopia (HP:0000662); Photophobia (HP:0000613); Visual field defect (HP:0001123); Nystagmus (HP:0000639); Intellectual disability (HP:0001249); Global developmental delay (HP:0001263); Optic atrophy (HP:0000648) Inheritance Familial, autosomal dominant Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Owner name Jinu Han Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Jinu Han Date created 2021-08-09 04:49:43 +02:00 (CEST) Date last edited 2021-12-08 15:42:39 +01:00 (CET)

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