Phenotype #0000292097

Individual ID 00399009
Associated disease NMD
Diagnosis/Initial congenital myopathy
Diagnosis/Definite -
Phenotype details serum CK <200 U/L; muscle biopsy central cores; hypotonia
Inheritance Familial, X-linked recessive
Age/Examination -
Age/Diagnosis -
Age/Onset <00y01m
Phenotype/Onset -
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 2022-01-15 16:40:49 +01:00 (CET)
Date last edited 2022-01-15 17:02:46 +01:00 (CET)

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