Phenotype #0000084106

Individual ID 00106291
Associated disease CMYO2A;NEM3
Phenotype details severe; contractures, no spontaneous movement at birth
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 2m
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Alan Beggs
Database submission license No license selected
Created by Alan Beggs
Date created 2007-11-16 13:32:20 +01:00 (CET)
Date last edited 2012-03-09 19:32:06 +01:00 (CET)

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