Global Variome shared LOVD

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

Phenotype #0000155299 Individual ID 00207521 Associated disease BVVLS1 Phenotype details Visual impairment (HP:0000505) Hearing impairment (HP:0000365) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite BVVLS Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Gunnar Schmidt Database submission license Creative Commons Attribution 4.0 International Created by Gunnar Schmidt Date created 2018-11-23 18:16:47 +01:00 (CET) Date last edited 2018-11-23 19:28:06 +01:00 (CET)

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