Global Variome shared LOVD

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Phenotype #0000308705 Individual ID 00417195 Associated disease AOS2 Phenotype details microcephaly (<3rd centile, HP:0000252), aplasia cutis congenita scalp (HP:0007385), global developmental delay (HP:0001263) Diagnosis/Initial Adams-Oliver syndrome Inheritance Familial, autosomal recessive Diagnosis/Definite AOS2 Age/Examination 02y (2 years) Age/Diagnosis 04y Age/Onset 00y Phenotype/Onset - Protein - Owner name Martin Zenker Database submission license Creative Commons Attribution 4.0 International Created by Martin Zenker Date created 2022-09-13 17:04:03 +02:00 (CEST) Date last edited 2022-09-14 15:43:51 +02:00 (CEST)

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