Phenotype #0000209190

Individual ID 00274228
Associated disease OPPG
Phenotype details bilateral retinal detachment (HP:0000541), severe osteopenia (HP:0000938)
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite osteoporosis-pseudoglioma syndrome
Age/Examination 08y (8 years)
Age/Diagnosis -
Age/Onset 01y
Phenotype/Onset retinal detachment (HP:0000541)
Protein -
Owner name Jasmine Chen
Database submission license No license selected
Created by Jasmine Chen
Date created 2019-12-27 16:41:10 +01:00 (CET)
Date last edited 2020-01-10 09:43:05 +01:00 (CET)

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