Phenotype #0000106133

Individual ID 00133386
Associated disease LGMDR5;LGMD2C
Phenotype details 1108 elevated CPK (HP:0003236)
Diagnosis/Initial severe autosomal recessive muscular dystrophy, North African type (SCARMD)
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 15y
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 2007-07-02 13:52:56 +02:00 (CEST)
Date last edited 2012-03-09 19:39:26 +01:00 (CET)

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