{"limit":20,"offset":0,"total":4,"items":[{"id":"MONDO:0018979","category":"biolink:Disease","name":"multifocal motor neuropathy","description":"Multifocal motor neuropathy (MMN) is a rare acquired immune-mediatedneuropathy characterized clinically by a purely motor deficit with conduction block and asymmetric multifocal weakness, fasciculations, and cramping.","xref":["GARD:0011011","ICD10CM:G61.82","ICD9:357.89","MEDGEN:581615","NANDO:1200031","NORD:1952","Orphanet:641","SCTID:230591002","UMLS:C0393847"],"synonym":["MMN","MMNCB","multifocal motor neuropathy with conduction block"],"exact_synonym":["MMN","MMNCB","multifocal motor neuropathy with conduction block"],"broad_synonym":null,"narrow_synonym":null,"related_synonym":null,"deprecated":null,"in_taxon":null,"in_taxon_label":null,"iri":null,"same_as":null,"subsets":["gard_rare","nord_rare","ordo_disorder","orphanet_rare","rare"],"file_source":"phenio_nodes","provided_by":"phenio_nodes","full_name":null,"symbol":null,"has_gene":null,"type":null,"has_attribute":null,"has_biological_sex":null,"synonyms":null,"namespace":"MONDO","has_phenotype":null,"has_phenotype_label":null,"has_phenotype_count":null,"has_phenotype_closure":null,"has_phenotype_closure_label":null,"has_descendant":null,"has_descendant_label":null,"has_descendant_count":null,"score":92.71881,"matched_field":"name","match_type":"exact","highlighting":{"name":["<em>multifocal</em> <em>motor</em> <em>neuropathy</em>"],"description":["<em>Multifocal</em> <em>motor</em> <em>neuropathy</em> (MMN) is a rare acquired immune-mediatedneuropathy characterized"],"synonym":["<em>multifocal</em> <em>motor</em> <em>neuropathy</em> with conduction block"]}},{"id":"MONDO:0018826","category":"biolink:Disease","name":"Lewis-Sumner syndrome","description":"A rare acquired demyelinating polyneuropathy characterized by asymmetrical distal weakness of the upper or lower extremities and motor dysfunction with adult onset. It is considered to be a variant of chronic inflammatory demyelinating polyneuropathy.","xref":["GARD:0013070","MEDGEN:798498","MedDRA:10065580","Orphanet:48162","UMLS:C1695985"],"synonym":["MADSAM","multifocal acquired demyelinating sensory and motor neuropathy"],"exact_synonym":["MADSAM","multifocal acquired demyelinating sensory and motor neuropathy"],"broad_synonym":null,"narrow_synonym":null,"related_synonym":null,"deprecated":null,"in_taxon":null,"in_taxon_label":null,"iri":null,"same_as":null,"subsets":["gard_rare","nord_rare","ordo_subtype_of_a_disorder","rare"],"file_source":"phenio_nodes","provided_by":"phenio_nodes","full_name":null,"symbol":null,"has_gene":null,"type":null,"has_attribute":null,"has_biological_sex":null,"synonyms":null,"namespace":"MONDO","has_phenotype":null,"has_phenotype_label":null,"has_phenotype_count":null,"has_phenotype_closure":null,"has_phenotype_closure_label":null,"has_descendant":null,"has_descendant_label":null,"has_descendant_count":null,"score":21.7015,"matched_field":null,"match_type":null,"highlighting":{"description":[" upper or lower extremities and <em>motor</em> dysfunction with adult onset. It is considered to be a variant of"],"synonym":["<em>multifocal</em> acquired demyelinating sensory and <em>motor</em> <em>neuropathy</em>"]}},{"id":"MONDO:0017362","category":"biolink:Disease","name":"neuralgic amyotrophy","description":"Neuralgic amyotrophy (NA) is an uncommon disorder of the peripheral nervous system characterized by the sudden onset of extreme pain in the upper extremity followed by rapid multifocal motor weakness and atrophy and a slow recovery in months to years. NA includes both an idiopathic (INA, also known as Parsonage-Turner syndrome) and hereditary (HNA) form.","xref":["GARD:0004228","ICD10CM:G54.5","MEDGEN:307145","MedDRA:10063020","NORD:1560","Orphanet:2901","SCTID:26609002","UMLS:C1510479","icd11.foundation:302246011"],"synonym":["Parsonage Turner Syndrome","acute brachial plexus neuritis","brachial plexus neuritis","immune brachial plexus neuropathy","mononeuritis multiplex with brachial predilection","neuralgic shoulder amyotrophy"],"exact_synonym":["Parsonage Turner Syndrome","acute brachial plexus neuritis","immune brachial plexus neuropathy","mononeuritis multiplex with brachial predilection","neuralgic shoulder amyotrophy"],"broad_synonym":["brachial plexus neuritis"],"narrow_synonym":null,"related_synonym":null,"deprecated":null,"in_taxon":null,"in_taxon_label":null,"iri":null,"same_as":null,"subsets":["clingen","gard_rare","nord_rare","ordo_disorder","orphanet_rare","otar","rare"],"file_source":"phenio_nodes","provided_by":"phenio_nodes","full_name":null,"symbol":null,"has_gene":null,"type":null,"has_attribute":null,"has_biological_sex":null,"synonyms":null,"namespace":"MONDO","has_phenotype":null,"has_phenotype_label":null,"has_phenotype_count":null,"has_phenotype_closure":null,"has_phenotype_closure_label":null,"has_descendant":null,"has_descendant_label":null,"has_descendant_count":null,"score":10.0929365,"matched_field":null,"match_type":null,"highlighting":{"description":[" the sudden onset of extreme pain in the upper extremity followed by rapid <em>multifocal</em> <em>motor</em> weakness"],"synonym":["immune brachial plexus <em>neuropathy</em>"]}},{"id":"MONDO:0006888","category":"biolink:Disease","name":"paraneoplastic polyneuropathy","description":"A diffuse or multifocal peripheral neuropathy caused by the effects of a distant neoplasm. It may be attributed, in part, to the immune response to neoplasm-elaborated proteins. The neuropathy may be sensory, motor, mixed or autonomic. It may be the initial presentation of an occult neoplasm. Detection and resection of the neoplasm may result in cure.","xref":["DOID:8681","GARD:0024499","ICD9:357.3","MEDGEN:124380","MESH:D020364","MedDRA:10062289","NCIT:C3981","SCTID:77659000","UMLS:C0270932"],"synonym":["paraneoplastic polyneuropathy"],"exact_synonym":["paraneoplastic polyneuropathy"],"broad_synonym":null,"narrow_synonym":null,"related_synonym":null,"deprecated":null,"in_taxon":null,"in_taxon_label":null,"iri":null,"same_as":null,"subsets":["gard_rare","rare"],"file_source":"phenio_nodes","provided_by":"phenio_nodes","full_name":null,"symbol":null,"has_gene":null,"type":null,"has_attribute":null,"has_biological_sex":null,"synonyms":null,"namespace":"MONDO","has_phenotype":null,"has_phenotype_label":null,"has_phenotype_count":null,"has_phenotype_closure":null,"has_phenotype_closure_label":null,"has_descendant":null,"has_descendant_label":null,"has_descendant_count":null,"score":7.29427,"matched_field":null,"match_type":null,"highlighting":{"description":["A diffuse or <em>multifocal</em> peripheral <em>neuropathy</em> caused by the effects of a distant neoplasm. It may"]}}],"facet_fields":[{"label":"category","facet_values":[{"label":"biolink:Disease","count":4}]},{"label":"in_taxon_label","facet_values":[]}],"facet_queries":[],"scope":null}