Phenotype #0000020388

Individual ID 00024269
Associated disease ID
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Isolated (sporadic)
Phenotype details severe intellectual disability, no epilepsy, axial hypotonia/peripheral
spasticity; MRI mild atrophy of the vermian region of cerebellum
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 2014-11-14 19:17:05 +01:00 (CET)
Date last edited N/A

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