Global Variome shared LOVD

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

Phenotype #0000242453 Individual ID 00320665 Associated disease OI Phenotype details Osteogenesis imperfecta Type 1, subtype A (presence of dentinogenesis imperfecta), Diagnosis/Initial - Inheritance - Diagnosis/Definite - Age/Examination - Age/Onset - Phenotype/Onset - Protein - Owner name Raymond Dalgleish Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Raymond Dalgleish Date created 2011-11-02 10:22:01 +01:00 (CET) Date last edited N/A

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