Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000359512 Individual ID 00474719 Associated disease ? Diagnosis/Initial Feingold syndrome Diagnosis/Definite FGLDS1 Phenotype details see paper; ..., microcephaly, OFC 52cm (<−2SD), fifth finger clinodactyly, partial syndactyly second to third/fourth to fifth toes; spontaneous abortion; no intellectual disability 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

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.