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: abdominal tuberculosis (MONDO:0000369)
Parent Node: kidney disease (MONDO:0005240)
Parent Node: urinary tract infection (disease) (MONDO:0005247)
Parent Node: urogenital tuberculosis (MONDO:0006002)
..Starting node ..renal tuberculosis ()
Child Nodes:
Sister Nodes:
..male genital tuberculosis ()
..renal tuberculosis ()
..tuberculous oophoritis ()
..tuberculous salpingitis ()
..ureter tuberculosis ()
..urinary bladder tuberculosis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5938
Name:	renal tuberculosis
Definition:	Infection of the kidney due to mycobacteria.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	kidney tuberculosis; tuberculosis of kidney
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal