Phenotype #0000153639

Individual ID 00205462
Associated disease XMPMA;EDMD6
Phenotype details -
Diagnosis/Initial myopathy, X-linked, with postural muscle atrophy
Inheritance Familial
Diagnosis/Definite XMPMA
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein WB FHL1 near absent
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 2009-09-11 20:47:21 +02:00 (CEST)
Date last edited 2012-03-04 15:57:33 +01:00 (CET)

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