Phenotype #0000273175

Individual ID 00378029
Associated disease LCA
Phenotype details HP:0000662, HP:0001129, HP:0000007, HP:0000639, HP:0001141, HP:0001483
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 2021-08-03 09:11:27 +02:00 (CEST)
Date last edited 2021-08-06 16:29:11 +02:00 (CEST)

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