Phenotype #0000203968

Individual ID 00266191
Associated disease ?
Diagnosis/Initial Pelizaeus-Merzbacher (like) disease
Diagnosis/Definite -
Phenotype details 10d-nystagmus, resolved 12m; 26m-walk, normal language development, no myopia; unclear pronunciation
Inheritance Familial, autosomal dominant
Age/Examination 5y (5 years)
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 2019-10-16 03:56:50 +02:00 (CEST)
Date last edited N/A

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