Phenotype #0000337251

Individual ID 00448062
Associated disease EDS
Inheritance Familial, autosomal recessive
Diagnosis/Initial Ehlers-Danlos syndrome VI
Age/Examination -
Diagnosis/Definite -
Age/Onset -
Phenotype/Onset -
Phenotype details see paper; ..., corneal rupture; myopia; blue sclera; no keratoconus; no keratoglobus; no poor healing/abnormal scarring; no soft skin/easy bruising; treatment for developmental dysplasia hip; no femoral epiphyseal changes; no scoliosis; small joint hypermobility; no fractures; no myalgia; no abnormal gait; no deafness; sclerocornea; cornea plana
Hearing/Loss -
Protein -
CK-level -
EMG -
Muscle/Biopsy -
Age/Diagnosis -
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 2024-02-14 13:52:54 +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.