Global Variome shared LOVD

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Phenotype #0000359586 Individual ID 00474793 Associated disease FGLDS1 Phenotype details see paper; ..., microcephaly (10m-OFC <3rd); mild generalized hypotonia; prominent metopic suture, ocular hypotelorism, low set ears, depressed nasal bridge, bilateral clinodactyly fifth fingers, cutaneous syndactyly multiple toes; bronchiolitis, otitis media, atopic dermatitis Diagnosis/Initial Feingold syndrome Inheritance Isolated (sporadic) Diagnosis/Definite FGLDS1 Age/Examination 01y01m (1 year, 1 month) 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 2026-03-25 21:45:41 +01:00 (CET) Date last edited N/A

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