Phenotype #0000315811

Individual ID 00424613
Associated disease EDS
Inheritance Familial, autosomal dominant
Diagnosis/Initial -
Age/Examination -
Diagnosis/Definite COL1-related overlap disorder
Age/Onset -
Phenotype/Onset -
Phenotype details -
Hearing/Loss -
Protein -
CK-level -
EMG -
Muscle/Biopsy -
Age/Diagnosis -
Owner name Marco Ritelli
Database submission license Creative Commons Attribution-ShareAlike 4.0 InternationalCreative Commons License
Created by Marco Ritelli
Date created 2022-11-21 11:36:16 +01:00 (CET)
Date last edited 2022-11-21 14:19:43 +01:00 (CET)

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