MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

Hello! Guest! Please Login or Register! Clinician Mode

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: skeletal tuberculosis (MONDO:0005962)
Parent Node: vertebral column disease (MONDO:0000812)
..Starting node ..tuberculosis, spinal ()
Child Nodes:
Sister Nodes:
..Baastrup syndrome ()
..coccygodynia ()
..epidural spinal canal neoplasm ()
..lumbosacral lipoma ()
..sacrococcygeal teratoma ()
..sacrum chordoma ()
..spinal injury ()
..spinal stenosis ()
..spondylocostal dysostosis ()
..tuberculosis, spinal ()
..vertebral disease ()
..vertebral joint disease ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	43836
Name:	tuberculosis, spinal
Definition:	Tuberculosis of the vertebrae.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	disease, pott; disease, pott's; pott disease; pott's disease; pott's paraplegia; Potts disease; spinal Tuberculoses; spinal tuberculosis; Tuberculoses, spinal; tuberculosis of spine (pott's); tuberculosis of vertebral column; tuberculosis of vertebral column - pott's; tuberculous spondylitis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal