Phenotype #0000324588

Individual ID 00434230
Associated disease ?
Diagnosis/Initial oculocutaneous albinism
Diagnosis/Definite HPS6
Phenotype details ocular albinism; hypoplasia of the fovea; exodeviation; hypermetropia; astigmatism
Inheritance Familial, autosomal recessive
Age/Examination 5y (5 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
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 2023-03-22 17:30:10 +01:00 (CET)
Date last edited N/A

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