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: hypertensive disorder (MONDO:0005044)
..Starting node ..essential hypertension ()
Child Nodes:
........benign essential hypertension ()
........essential hypertension, genetic ()
........malignant essential hypertension ()
Sister Nodes:
..chemotherapy-induced hypertension ()
..early onset hypertension ()
..essential hypertension ()
..genetic hypertension ()
..hypertension, pregnancy-induced ()
..intracranial hypertension ()
..kallikrein hypertension ()
..malignant hypertension ()
..ocular hypertension ()
..pulmonary hypertension ()
..resistant hypertension ()
..secondary hypertension ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1134
Name:	essential hypertension
Definition:	Hypertension that presents without an identifiable cause.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	idiopathic hypertension; primary hypertension
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal