Global Variome shared LOVD

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

Phenotype #0000242456 Individual ID 00320669 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 Katarina Lindahl Database submission license No license selected Created by Katarina Lindahl Date created 2014-12-08 13:35:32 +01:00 (CET) Date last edited 2015-08-07 14:28:13 +02:00 (CEST)

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