Phenotype #0000242972

Individual ID 00324430
Associated disease OCA1
Phenotype details Subclinical nystagmus, Grade 1 foveal hypoplasia,
Diagnosis/Initial Albinism
Inheritance Familial, autosomal recessive
Diagnosis/Definite Albinism
Age/Examination 05y (5 years)
Age/Diagnosis 05y
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Mervyn Thomas
Database submission license No license selected
Created by Mervyn Thomas
Date created 2020-12-12 11:25:16 +01:00 (CET)
Date last edited 2020-12-13 10:46:27 +01:00 (CET)

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