Global Variome shared LOVD

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Phenotype #0000237090 Individual ID 00311842 Associated disease RRS Phenotype details severe brachydactyly (BDB1); patient BDB_005 has deletion of the same region Diagnosis/Initial Robinow syndrome Inheritance - Diagnosis/Definite RRS1 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Jacopo Celli Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Jacopo Celli Date created 2010-04-28 12:53:12 +02:00 (CEST) Date last edited 2010-04-29 08:54:58 +02:00 (CEST)

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