Phenotype #0000273478

Individual ID 00379634
Associated disease LCA
Phenotype details HP:0001483, HP:0001263, HP:0032122, HP:0000007, HP:0000639
Diagnosis/Initial Leber congenital amaurosis (LCA)
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Jinu Han
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Jinu Han
Date created 2021-08-06 04:04:10 +02:00 (CEST)
Date last edited 2021-08-06 19:34:52 +02:00 (CEST)

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