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: spondyloarthropathy (MONDO:0005095)
..Starting node ..hypermobility of coccyx ()
Child Nodes:
Sister Nodes:
..ankylosing spondylitis ()
..hypermobility of coccyx ()
..Kummell disease ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1546
Name:	hypermobility of coccyx
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	coccygeal hypermobility syndrome; hypermobility of the coccyx
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal