Phenotype #0000308876

Individual ID 00417389
Associated disease ROP
Phenotype details -
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite retinopathy of prematurity
Age/Examination -
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 2022-09-15 20:29:02 +02:00 (CEST)
Date last edited N/A

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