Phenotype #0000246736

Individual ID 00328510
Associated disease -
Phenotype details retinal dystrophy (HP:0000556), neurodevelopmental abnormality (HP:0012759), abnormal facial shape (HP:0001999)
Diagnosis/Initial retinal dystrophy
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 3y (3 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-01-28 09:35:56 +01:00 (CET)
Date last edited N/A

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