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| Gastrointestinal neuromuscular disease v0.14 | NRTN | Bryony Thompson Marked gene: NRTN as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Gastrointestinal neuromuscular disease v0.14 | NRTN | Bryony Thompson Gene: nrtn has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Gastrointestinal neuromuscular disease v0.14 | NRTN |
Bryony Thompson gene: NRTN was added gene: NRTN was added to Gastrointestinal neuromuscular disease. Sources: Expert list Mode of inheritance for gene: NRTN was set to Unknown Publications for gene: NRTN were set to 21206993; 10069332; 9700200 Phenotypes for gene: NRTN were set to Hirschsprung disease Review for gene: NRTN was set to RED Added comment: A mouse model has a gastrointestinal neuromuscular phenotype, however there is limited evidence that variants in NRTN cause Hirschsprung disease or a gastrointestinal neuromuscular disease in humans. Sources: Expert list |
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