Phenotype #0000052021

Individual ID	00072352
Associated disease	CCTRCT
Phenotype details	bilateral opacification of the lens (HP:?), anterior axial embryonal nuclear cataract (HP:?), no pathological findings of the anterior or posterior chamber structures (-HP:?)
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Jamie Zeegers
Database submission license	No license selected
Created by	Jamie Zeegers
Date created	2016-06-06 13:56:04 +02:00 (CEST)
Date last edited	2016-06-26 19:14:41 +02:00 (CEST)

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