Global Variome shared LOVD

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

Phenotype #0000307366 Individual ID 00415586 Associated disease - Phenotype details Pseudodominant inheritance; mild myopia (?1.0 to ?2.0 D) with mild astigmatism; nystagmus and strabismus Diagnosis/Initial autosomal recessive congenital stationary night blindness (CSNB) Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2022-08-15 15:41:08 +02:00 (CEST) Date last edited N/A

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