Phenotype #0000345873

Individual ID 00457409
Associated disease MLID
Diagnosis/Initial Beckwith-Wiedemann syndrome (multilocus imprinting disturbances)
Diagnosis/Definite -
Phenotype details see paper; ..., omphalocele, macroglossia, neonatal hypoglycaemia, heart defect, developmental delay
Inheritance Unknown
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
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 2024-11-11 13:38:28 +01:00 (CET)
Date last edited N/A

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