Phenotype #0000291483

Individual ID 00398362
Associated disease -
Phenotype details night blindness; Mild cortical opacity
Diagnosis/Initial Choroidermia (CHM)
Inheritance Familial, X-linked
Diagnosis/Definite -
Age/Examination 53y (53 years)
Age/Diagnosis -
Age/Onset 20y-29y
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2022-01-05 04:00:26 +01:00 (CET)
Date last edited N/A

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