Global Variome shared LOVD

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

Phenotype #0000166010 Individual ID 00217560 Associated disease CCD Phenotype details scoliosis; facial weakness Diagnosis/Initial CCD; MHS1? Inheritance Familial, autosomal dominant Diagnosis/Definite CCD Age/Examination - Age/Diagnosis - Age/Onset 1d Phenotype/Onset bilateral congenital dislocation of the hips Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2009-11-01 22:02:21 +01:00 (CET) Date last edited 2017-03-31 14:13:45 +02:00 (CEST)

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