Global Variome shared LOVD

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Phenotype #0000020464 Individual ID 00024346 Associated disease ACG2 Phenotype details see paper; ..., hypochondrogenesis; remarkable phenotype radiographically by more metaphyseal involvement and clinically by absence of respiratory insufficiency in the postnatal period; died at 13m Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2012-01-08 15:07:53 +01:00 (CET) Date last edited 2016-12-06 13:08:38 +01:00 (CET)

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