Phenotype #0000053290

Individual ID 00072256
Associated disease CTRCT16;CTPP2
Phenotype details poor vision (HP:0000505), visual acuity test abnormality - before surgery (HP:0030532), less visual acuity test abnormality - after surgery (HP:0030532)
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 10y
Phenotype/Onset -
Protein -
Owner name Jamie Zeegers
Database submission license No license selected
Created by Jamie Zeegers
Date created 2016-06-02 16:09:37 +02:00 (CEST)
Date last edited 2016-06-12 14:07:00 +02:00 (CEST)

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