Global Variome shared LOVD

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Phenotype #0000312767 Individual ID 00421531 Associated disease - Phenotype details microcephaly at birth; global developmental delay with absent speech; mild asthma; hypotonia with spasticity in the lower extremities; computer tomography and electroencaphalography of the head: normal; ophthalmologic exam: normal Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination 5y (5 years) Age/Diagnosis 1y Age/Onset 0m Phenotype/Onset microcephaly Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2022-11-07 13:33:04 +01:00 (CET) Date last edited N/A

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