Phenotype #0000292406

Individual ID 00399289
Associated disease OI
Phenotype details -
Diagnosis/Initial osteogenesis imperfecta
Inheritance Familial, autosomal dominant
Diagnosis/Definite OI1
Age/Examination -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-01-18 21:42:12 +01:00 (CET)
Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.