Phenotype #0000086093

Individual ID 00108620
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details 50y-asymptomatic male, identified after incidental variant detection in a daughter affected with developmental delay
Inheritance Unknown
Age/Examination -
Age/Diagnosis 50y
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 2017-07-27 16:10:26 +02:00 (CEST)
Date last edited N/A

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