Global Variome shared LOVD

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

Phenotype #0000187325 Individual ID 00248327 Associated disease arthrogryposis Inheritance Familial, autosomal recessive Diagnosis/Initial severe arthrogryposis multiplex congenita Age/Examination - Diagnosis/Definite LCCS-9 Age/Diagnosis - Age/Onset - Phenotype/Onset - Phenotype details see paper; … Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2019-07-21 21:47:12 +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.