Phenotype #0000317626

Individual ID 00426471
Associated disease MCOP
Phenotype details left eye Peters Anomaly, microphthalmia; right eye hyperopia; bilateral nystagmus; mild developmental delay/learning difficulties
Diagnosis/Initial microphthalmia
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 07y (7 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-11-30 16:42:38 +01:00 (CET)
Date last edited N/A

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