Global Variome shared LOVD

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Phenotype #0000311609 Individual ID 00420341 Associated disease BBS Phenotype details smaller but supernumerary cilia and present abnormal accumulations of ciliary proteins Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite Meckel syndrome Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2022-11-01 11:33:46 +01:00 (CET) Date last edited N/A

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