Phenotype #0000326850

Individual ID 00436736
Associated disease LCA10
Phenotype details HP: 0007875 Congenital Amaurosis
Diagnosis/Initial LCA10
Inheritance Familial, autosomal recessive
Diagnosis/Definite # 611755
Age/Examination 00y04m (4 months)
Age/Diagnosis 04y
Age/Onset 00y04m
Phenotype/Onset 0y04m
Protein -
Owner name Rocio Villafuerte-de la Cruz
Database submission license Creative Commons Attribution-ShareAlike 4.0 InternationalCreative Commons License
Created by Rocio Villafuerte-de la Cruz
Date created 2023-09-29 22:07:00 +02:00 (CEST)
Date last edited 2023-10-01 21:07:59 +02:00 (CEST)

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