Phenotype #0000308383

Individual ID 00416873
Associated disease OPPG
Phenotype details no familial exudative vitreoretinopathy, no osteopenia; lumbar bone mineral density of 1.199 g/cm2 (Z-score: 1.4 SD)
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite osteoporosis-pseudoglioma syndrome (OPPG)
Age/Examination 31y (31 years)
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 2022-09-08 21:04:11 +02:00 (CEST)
Date last edited N/A

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