Global Variome shared LOVD

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Phenotype #0000288194 Individual ID 00394994 Associated disease LIS3 Phenotype details Increased nuchal translucency, Fetal cystic hygroma; the first-born daughter, 10 years old, showed global developmental delay and cerebellar vermis hypoplasia after premature birth in the 23rd week of gestation. Diagnosis/Initial 0y Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2021-12-03 11:50:11 +01:00 (CET) Date last edited 2021-12-03 13:55:12 +01:00 (CET)

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