Global Variome shared LOVD

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

Phenotype #0000242649 Individual ID 00323345 Associated disease OI Phenotype details Osteogenesis imperfacta Type 1, subtype B (absence 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 2014-12-05 13:33:35 +01:00 (CET) Date last edited 2015-08-07 15:26:29 +02:00 (CEST)

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