Phenotype #0000051969

Individual ID 00072264
Associated disease CCTRCT
Phenotype details no ocular abnormality (-HP:?), clinically insignificant fine opacities in the red reflect (HP:?)
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 01y
Phenotype/Onset -
Protein -
Owner name Jamie Zeegers
Database submission license No license selected
Created by Jamie Zeegers
Date created 2016-06-03 10:10:30 +02:00 (CEST)
Date last edited 2016-06-12 14:16:46 +02:00 (CEST)

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