MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: demyelinating disease (MONDO:0002562)
Parent Node: polyneuropathy (MONDO:0001824)
..Starting node ..polyradiculoneuropathy ()
Child Nodes:
........chronic inflammatory demyelinating polyradiculoneuropathy ()
........chronic polyradiculoneuritis ()
........chronic polyradiculoneuropathy ()
........polyradiculopathy ()
Sister Nodes:
..alcoholic polyneuropathy ()
..chronic polyneuropathy ()
..critical illness polyneuropathy ()
..demyelinating polyneuropathy ()
..idiopathic progressive polyneuropathy ()
..paraneoplastic polyneuropathy ()
..polyneuritis ()
..polyneuropathy due to drug ()
..polyneuropathy in collagen vascular disease ()
..polyradiculoneuropathy ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	6915
Name:	polyradiculoneuropathy
Definition:	Diseases characterized by injury or dysfunction involving multiple peripheral nerves and nerve roots. The process may primarily affect myelin or nerve axons. Two of the more common demyelinating forms are acute inflammatory polyradiculopathy (guillain-barre syndrome) and polyradiculoneuropathy, chronic inflammatory demyelinating. Polyradiculoneuritis refers to inflammation of multiple peripheral nerves and spinal nerve roots.
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Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal