Global Variome shared LOVD

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Phenotype #0000359511 Individual ID 00474718 Associated disease ? Diagnosis/Initial Feingold syndrome Diagnosis/Definite FGLDS1 Phenotype details see paper; ..., microcephaly, OFC 49.5cm (<−2SD), fifth finger clinodactyly, partial syndactyly second to third/fourth to fifth toes; spontaneous abortion; chronic nephritis syndrome, renal insufficiency; hypertension; no intellectual disability (IQ97) Inheritance Familial, autosomal dominant Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2026-03-24 19:23:04 +01:00 (CET) Date last edited N/A

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