Global Variome shared LOVD

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Phenotype #0000228474 Individual ID 00301206 Associated disease TCS1 Phenotype details The patient had malar hypoplasia, micrognathia, antimongoloid slanting palpebral fissures, malformed ears, and loss hearing Diagnosis/Initial UNKONGWN Inheritance Isolated (sporadic) Diagnosis/Definite TCS-1 Age/Examination 00y06m (6 months) Age/Diagnosis 00y08m Age/Onset 00y04m Phenotype/Onset malar hypoplasia, micrognathia, antimongoloid slanting palpebral fissures, malformed ears, and loss hearing Protein - Owner name Jinxiu Liu Database submission license Creative Commons Attribution 4.0 International Created by Jinxiu Liu Date created 2020-05-09 08:26:02 +02:00 (CEST) Date last edited 2020-05-19 14:44:26 +02:00 (CEST)

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