Global Variome shared LOVD

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Phenotype #0000039763 Individual ID 00053038 Associated disease SGS Phenotype details craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; no camptodactyly; no scoliosis; no pectus deformity; joint hypermobility; joint contracture; hypotonia; developmental delay; no mitral valve prolapse; no aortic root dilatation; no ectopia lentis; cleft palate; club foot deformity; splenic artery aneurysm with spontaneous rupture (blank cells, not determined) Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination 6y (6 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2015-10-29 22:56:24 +01:00 (CET) Date last edited N/A

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