Phenotype #0000053378

Individual ID 00073641
Associated disease CCTRCT
Phenotype details bilateral involvement (HP:?), abnormal red reflex (HP:?), specks in the nucleus of the lens (HP:?), clear peripheral and intervening lens (HP:?)
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 04y (4 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Jamie Zeegers
Database submission license No license selected
Created by Jamie Zeegers
Date created 2016-06-13 12:02:52 +02:00 (CEST)
Date last edited 2017-07-18 21:46:07 +02:00 (CEST)

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