Global Variome shared LOVD

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Phenotype #0000025774 Individual ID 00029801 Associated disease AOS Phenotype details see paper; syndactyly 2nd/3rd toes, otherwise normal, short palpebral fissures, mildly delayed gross motor milestones, microcephaly, aplasia cutis congenita scalp (HP:0007385) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 00y00m00d () 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 2015-02-08 20:54:44 +01:00 (CET) Date last edited 2023-03-03 13:48:07 +01:00 (CET)

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