| | | also see: nervous system heredodegenerative disorders, liver diseases, tuberous sclerosis, myotonic dystrophy, neurofibromatoses, movement disorders, basal ganglia diseases, inborn errors metal metabolism, myotonia congenita, cockayne syndrome |
| synonym: hepatic form of wilson disease, hepato neurologic wilson disease, hepatocerebral degeneration, kinnier wilson disease, progressive lenticular degeneration, westphal strumpell syndrome, hepatic form wilson disease, wilsons disease |
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| Top genes for hepatolenticular degeneration : |
| ATOX1 human also called: atx1 antioxidant protein 1 yeast homolog 1, atx1, copper transport, atox1, hah1, antioxidant protein 1, metal transport publications |
| ATP7A human also called: atpase cu transporting alpha polypeptide, copper transporting atpase 1, atp7a, mnk, otthump00000062077, menkes disease associated protein, copper pump 1, ohs publications |
| ATP7B human also called: otthump00000040880, atpase cu transporting beta polypeptide wilson disease, copper pump 2, atpase cu 2 transporting beta polypeptide, wnd, pwd, wilson disease associated, wc1, atp7b, atpase cu transporting beta polypeptide, copper transporting atpase 2, wd protein publications |
| Atp7a rat also called: atpase cu transporting alpha polypeptide, atp7a, mnk, atpase cu transporting alpha polypeptide menkes syndrome publications |
| Atp7b rat also called: pina gene promoter, atpase cu transporting beta polypeptide same as wilson disease, atp7b, atpase cu transporting beta polypeptide, pina, hts publications |
| CCC2 baker's yeast also called: ccc2p, cu 2 transporting ptype atpase required for export of copper from the cytosol into an extracytosolic compartment has similarity to human proteins involved in menkes and wilsons diseases, ccc2 publications |
| CLCN4 human also called: clcn4, chloride channel 4, clc4a, clc4 publications |
| COMMD1 human also called: mgc27155, chromosome 2 open reading frame 5 murr1, c2orf5, copper metabolism gene murr1, commd1, murr1 publications |
| CP human also called: ceruloplasmin, ceruloplasmin ferroxidase, ferroxidase publications |
| DGKG human also called: mgc104993, dgk gamma, diacylglycerol kinase gamma 90kda, diacylglycerol kinase gamma 90kd, dgkg, dagk3 publications |
| Dbh mouse also called: dopamine beta hydroxylase, dbh publications |
| Esd mouse also called: esd, es10, sid478, esterase d formylglutathione hydrolase, esterase 10 publications |
| LOX human also called: lox, protein lysine 6oxidase, lysyl oxidase, mgc105112 publications |
| LOXL2 human also called: ws914, lor2, lysyl oxidase homolog 2, loxl2, lysyl oxidase like 2, lysyl oxidase related 2 publications |
| NOS2A human also called: nos, nitric oxide synthase macrophage, nos2, nitric oxide synthase 2a, nos type ii, hep nos, nos2a, inos publications |
| PNOC human also called: pnoc, propronociceptin, prepronociceptin, ppnoc publications |
| Rb1 mouse also called: rb1, retinoblastoma 1, prb publications |
| TNFRSF11B human also called: mgc29565, osteoprotegerin, tr1, osteoclastogenesis inhibitory factor, opg, ocif, tnfrsf11b publications |
| Top webpages for hepatolenticular degeneration: more are being identified and will be added. |
1. liver information: hepatolenticular degeneration caused by e ...
www.surgery.usc.edu/divisions/hep/livernewsletter-wilsondise ... |
2. hardin md : wilsons disease / wilson's disease
www.lib.uiowa.edu/hardin/md/wilsonsdisease.html |
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