Phenotype #0000235217

Individual ID 00309899
Associated disease PBD
Phenotype details see paper; ...,severe cholestasis, hepatomegaly, neuronal migration defect, progressive hypotonia
Diagnosis/Initial Zellweger syndrome
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
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 2008-01-31 08:48:00 +01:00 (CET)
Date last edited 2020-09-06 09:53:58 +02:00 (CEST)

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