Phenotype #0000015234

Individual ID 00016720
Associated disease DA5
Phenotype details contractures hand/feet; III7 mild ptosis; ophthalmoplegia (except II6); I2/II2/II5 pulmonary disease
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Marianne Vos (LOVD-team)
Database submission license No license selected
Created by Marianne Vos (LOVD-team)
Date created 2014-05-27 13:26:55 +02:00 (CEST)
Date last edited 2015-09-11 19:47:11 +02:00 (CEST)

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