Phenotype #0000117233

Individual ID 00144496
Associated disease CNM2
Phenotype details wheelchair-bound 13y
Diagnosis/Initial myopathy, centronuclear
Inheritance Unknown
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 2010-11-14 17:33:43 +01:00 (CET)
Date last edited 2017-12-15 11:23:09 +01:00 (CET)

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