Phenotype #0000333629

Individual ID 00444376
Associated disease MCOP
Phenotype details see paper; ..., bilateral anophthalmia I; intellectual deficiency, autistic features; brother isolated unilateral iris coloboma, bilateral severe myopia
Diagnosis/Initial microphthalmia
Inheritance Familial
Diagnosis/Definite MCOPCB10
Age/Examination -
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 2023-12-23 17:05:31 +01:00 (CET)
Date last edited N/A

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