Individual #00002929

ID_report -
Reference PubMed: Lossos 2013
Remarks 22 affecteds from 8 families
Gender -
Consanguinity yes
Country Israel
Population Arab
Age at death -
VIP -
Data_av -
Treatment -
Panel size 22
Diseases CMYO6
Owner name Homa Tajsharghi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-09-19 19:25:22 +02:00 (CEST)
Date last edited N/A


Phenotypes

myopathy, congenital, type 6, with ophthalmoplegia (CMYO6;MYPOP)   Add phenotype for this disease

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Owner     
0000001836 external ophthalmoplegia; conjugate non-restrictive ocular motility impairment, no ptosis, mild facial/limb muscle weakness, scoliosis; skeletal muscle biopsy marked type 1 fibre predominance - - Familial, autosomal recessive - - - - - Homa Tajsharghi


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