Phenotype #0000310193

Individual ID 00380724
Associated disease ?
Diagnosis/Initial basal ganglia anomalies, exudative vitreoretinopathy
Diagnosis/Definite -
Phenotype details see paper; ..., basal ganglia anomalies, exudative vitreoretinopathy
Inheritance Familial, autosomal recessive
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
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 2022-10-12 09:45:42 +02:00 (CEST)
Date last edited N/A

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