Phenotype #0000125565

Individual ID 00152636
Associated disease LIS
Diagnosis/Initial lissencephaly, type II
Diagnosis/Definite -
Phenotype details 22w pregnancy termination because of reoccurrence severe quadriventricular hydrocephalus/cerebellar hypoplasia (like fetus F1); fetus dysmorphic features, horizontal narrow palpebral slit, bulging eyes, hypertrichosis cheeks/shoulders
Inheritance Isolated (sporadic)
Age/Examination -
Age/Onset <0d
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2012-04-22 00:16:26 +02:00 (CEST)
Date last edited N/A

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