Global Variome shared LOVD

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

Phenotype #0000273649 Individual ID 00379794 Associated disease OCMD Phenotype details HP:0030515, HP:0001123, HP:0030636, HP:0011003 Diagnosis/Initial dystrophy, macular, occult (OCMD) Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Jinu Han Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Jinu Han Date created 2021-08-10 03:19:35 +02:00 (CEST) Date last edited 2021-08-11 14:39:17 +02:00 (CEST)

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