Phenotype #0000275978

Individual ID 00382136
Associated disease LCA2
Phenotype details retinal dystrophy; MIM, 204100 or 613794
Diagnosis/Initial MIM, 204100 or 613794
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2021-09-07 10:12:12 +02:00 (CEST)
Date last edited N/A

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