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: essential hypertension (MONDO:0001134)
..Starting node ..benign essential hypertension ()
Child Nodes:
Sister Nodes:
..benign essential hypertension ()
..essential hypertension, genetic ()
..malignant essential hypertension ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1151
Name:	benign essential hypertension
Definition:	A condition of mild to moderate high blood pressure that has no identifiable cause.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign essential hypertension
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal