Phenotype #0000023245

Individual ID 00027174
Associated disease NEM
Phenotype details typical congenital nemaline myopathy; alive (4y); polyhydramnios, bulbar weakness, percutaneous endoscopic gastrostomy, nocturnal noninvasive ventilation; walks with truncal support; nNormal cardiac assessment and echocardiogram
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 2014-12-22 16:45:30 +01:00 (CET)
Date last edited N/A

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