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| Pain syndromes v0.3 | SCN9A | Zornitza Stark Added phenotypes HSAN2D, autosomal recessive, AR, 243000; Erythermalgia, primary, AD, 133020; Insensitivity to pain, congenital, AR, 243000; Small fiber neuropathy, AD,133020; Paroxysmal extreme pain disorder, AD, 167400 for gene: SCN9A | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Pain syndromes v0.0 | SCN9A |
Zornitza Stark gene: SCN9A was added gene: SCN9A was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green Mode of inheritance for gene: SCN9A was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: SCN9A were set to 16392115; 17167479; 17470132; 17145499; 17679678; 25316021; 15958509; 28665811; 23596073; 24817410; 28235406; 16216943; 24813307; 14985375; 1536168 Phenotypes for gene: SCN9A were set to HSAN2D, autosomal recessive, AR, 243000; Erythermalgia, primary, AD, 133020; Insensitivity to pain, congenital, AR, 243000; Small fiber neuropathy, AD,133020; Paroxysmal extreme pain disorder, AD, 167400 |
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