Phenotype #0000280732

Individual ID 00386933
Associated disease MRD26
Phenotype details Intellectual disability/developmental delay, structural brain anomaly, cerebral palsy/spasticity, white matter abnormalities, ptosis, strabismus
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination 03y (3 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Birth_Details -
Protein -
Owner name Alexander Groffen
Database submission license Creative Commons Attribution-ShareAlike 4.0 InternationalCreative Commons License
Created by Alexander Groffen
Date created 2021-10-27 14:55:36 +02:00 (CEST)
Date last edited N/A

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