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| Gastrointestinal neuromuscular disease v0.18 | NRG3 | Bryony Thompson Marked gene: NRG3 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Gastrointestinal neuromuscular disease v0.18 | NRG3 | Bryony Thompson Gene: nrg3 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Gastrointestinal neuromuscular disease v0.18 | NRG3 |
Bryony Thompson gene: NRG3 was added gene: NRG3 was added to Gastrointestinal neuromuscular disease. Sources: Expert list Mode of inheritance for gene: NRG3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: NRG3 were set to 23315268 Phenotypes for gene: NRG3 were set to Hirschsprung disease Review for gene: NRG3 was set to RED Added comment: Single Chinese mother and son reported, and some sporadic cases that appear to have recurrent variants that may be polymorphisms. No functional evidence. Sources: Expert list |
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