Global Variome shared LOVD

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

Phenotype #0000222542 Individual ID 00288837 Associated disease HCIN Diagnosis/Initial hyperostosis cranialis interna Diagnosis/Definite HCIN Phenotype details see paper; ... Inheritance Familial, autosomal dominant Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2020-02-22 10:13:34 +01:00 (CET) Date last edited 2020-02-22 10:16:11 +01:00 (CET)

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