Global Variome shared LOVD

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Phenotype #0000142305 Individual ID 00179851 Associated disease CDLS Phenotype details facial anomalies; speech 24m-48m; hirsutism; intra uterine growth retardation; small hands; no microcephaly; walking 18m-42m; post natal growth retardation; urinary anomalies Diagnosis/Initial Cornelia de Lange syndrome Inheritance Isolated (sporadic) Diagnosis/Definite CDLS-1 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Cristina Dias Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Jorge Oliveira Date created 2011-06-06 12:16:10 +02:00 (CEST) Date last edited N/A

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