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| Cardiomyopathy_Paediatric v1.10 | FXN_FRDA_GAA | Zornitza Stark Marked STR: FXN_FRDA_GAA as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiomyopathy_Paediatric v1.10 | FXN_FRDA_GAA | Zornitza Stark Str: fxn_frda_gaa has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiomyopathy_Paediatric v1.10 | Zornitza Stark Copied STR FXN_FRDA_GAA from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiomyopathy_Paediatric v1.10 | FXN_FRDA_GAA |
Zornitza Stark STR: FXN_FRDA_GAA was added STR: FXN_FRDA_GAA was added to Cardiomyopathy_Paediatric. Sources: Expert list,Expert Review Green,Expert Review Green,Expert list paediatric-onset tags were added to STR: FXN_FRDA_GAA. Mode of inheritance for STR: FXN_FRDA_GAA was set to BIALLELIC, autosomal or pseudoautosomal Publications for STR: FXN_FRDA_GAA were set to 20301458; 8596916 Phenotypes for STR: FXN_FRDA_GAA were set to Friedreich ataxia MIM#229300 |
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| Cardiomyopathy_Paediatric v1.9 | FXN | Zornitza Stark Marked gene: FXN as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiomyopathy_Paediatric v1.9 | FXN | Zornitza Stark Gene: fxn has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiomyopathy_Paediatric v1.9 | FXN | Zornitza Stark Classified gene: FXN as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiomyopathy_Paediatric v1.9 | FXN | Zornitza Stark Gene: fxn has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiomyopathy_Paediatric v1.8 | FXN | Zornitza Stark Tag STR tag was added to gene: FXN. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiomyopathy_Paediatric v1.8 | FXN |
Zornitza Stark gene: FXN was added gene: FXN was added to Cardiomyopathy_Paediatric. Sources: Expert Review Mode of inheritance for gene: FXN was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: FXN were set to 41432640; 40880907; 38396238; 34610949; 32999401 Phenotypes for gene: FXN were set to Friedreich ataxia, MIM# 229300 Review for gene: FXN was set to GREEN Added comment: Well established gene-disease association. Hypertrophic cardiomyopathy is a feature. Onset in adolescence/childhood. Sources: Expert Review |
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