Phenotype #0000272049

Individual ID 00376839
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details see paper; ..., global developmental delay, generalized muscular hypotonia, visual dysfunction
Inheritance Unknown
Age/Examination 00y23m (23 months)
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 2021-06-25 16:09:30 +02:00 (CEST)
Date last edited N/A

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