Phenotype #0000357049

Individual ID 00472240
Associated disease -
Phenotype details 0003198: Myopathy, 0004887: Respiratory failure requiring ventilatory support
Diagnosis/Initial Myopathy
Inheritance Unknown
Diagnosis/Definite Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Camille Verebi
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Camille Verebi
Date created 2026-01-19 16:36:38 +01:00 (CET)
Date last edited 2026-02-06 10:21:15 +01:00 (CET)

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