Phenotype #0000027612

Individual ID 00034216
Associated disease -
Phenotype details see paper; infantile-onset neurodegenerative disorder, predominant
sensorimotor axonal neuropathy, optic atrophy, cognitive deficit
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
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 2015-03-13 20:18:28 +01:00 (CET)
Date last edited N/A

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