Global Variome shared LOVD

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Phenotype #0000358805 Individual ID 00474010 Associated disease ? Diagnosis/Initial hemifacial microsomia Diagnosis/Definite - Phenotype details see paper; ..., hemifacial microsomia; mandibular hypoplasia, moderate to severe conductive hearing loss; ear deformities (some memebrs) Inheritance Familial, autosomal dominant Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2026-03-07 15:17:19 +01:00 (CET) Date last edited N/A

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