Phenotype #0000052859

Individual ID 00073191
Associated disease CCTRCT
Phenotype details bilateral nuclear cataracts (HP:0000519), microcornea (HP:0000482), nystagmus (HP:0000639), amblyopia (HP:0000646)
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis 13y
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Jamie Zeegers
Database submission license No license selected
Created by Jamie Zeegers
Date created 2016-06-09 15:15:40 +02:00 (CEST)
Date last edited 2017-07-18 21:30:32 +02:00 (CEST)

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