{"orpha":98505,"name":"Genetic motor neuron disease","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Genetic anterior horn cell disease"],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-98505/","orphanet_url":"https://www.orpha.net/en/disease/detail/98505","names":{"fr":{"name":"Maladie génétique du motoneurone","synonyms":["Maladie génétique de la corne antérieure"]},"de":{"name":"Krankheit der Vorderhornzellen, autosomal-dominant oder rezessive"},"es":{"name":"Enfermedad genética de la motoneurona","synonyms":["Enfermedad de las células del cuerno anterior, autosómica dominante o recesiva"]},"it":{"name":"Malattia delle cellule delle corna anteriori, autosomica dominante o recessiva"},"nl":{"name":"Genetische motorneuronziekte","synonyms":["Genetische aandoening van voorhoorncellen"]},"pt":{"name":"Doença das células dos cornos anteriores, autossómica dominante ou autossómica recessiva"},"pl":{"name":"Genetyczna choroba neuronu ruchowego","synonyms":["Gentyczna choroba komórek przedniego rogu rdzenia"]},"cs":{"name":"Geneticky podmíněná onemocnění motoneuronů","synonyms":["Geneticky podmíněná onemocnění předních rohů míšních"]},"uk":{"name":"Генетично обумовлене захворювання мотонейронів","synonyms":["Генетичне захворювання клітин переднього рогу"]},"zh":{"name":"遗传性运动神经元病","synonyms":["遗传性前角细胞病"]},"tr":{"name":"Genetik motor nöron hastalığı","synonyms":["Genetik ön boynuz hücre hastalığı"]}},"xrefs":[{"source":"UMLS","code":"C5680368","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":183497,"name":"Genetic neuromuscular disease","classifications":[156]},{"orpha":98503,"name":"Motor neuron disease","classifications":[181]}],"children":[{"orpha":357043,"name":"Amyotrophic lateral sclerosis type 4","type":"Disease"},{"orpha":211037,"name":"Autosomal dominant proximal spinal muscular atrophy","type":"Clinical group"},{"orpha":206701,"name":"Bulbospinal muscular atrophy","type":"Category"},{"orpha":53739,"name":"Distal hereditary motor neuropathy","type":"Clinical group"},{"orpha":293168,"name":"Infantile-onset ascending hereditary spastic paralysis","type":"Disease"},{"orpha":300605,"name":"Juvenile amyotrophic lateral sclerosis","type":"Disease"},{"orpha":247604,"name":"Juvenile primary lateral sclerosis","type":"Disease"},{"orpha":137867,"name":"Madras motor neuron disease","type":"Disease"},{"orpha":85146,"name":"Neurogenic scapuloperoneal syndrome, Kaeser type","type":"Disease"},{"orpha":486811,"name":"Prenatal-onset spinal muscular atrophy with congenital bone fractures","type":"Disease"},{"orpha":70,"name":"Proximal spinal muscular atrophy","type":"Disease"},{"orpha":431255,"name":"Scapuloperoneal spinal muscular atrophy","type":"Disease"},{"orpha":2590,"name":"Spinal muscular atrophy-progressive myoclonic epilepsy syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}