Disease browser and phenotype 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

Disease Browser
Parent Node: Hypertension (D006973)
..Starting node ..White Coat Hypertension (D059466)
Child Nodes:
Sister Nodes:
..Adams Nance syndrome (C538224)
..Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly (C566529)
..Brachydactyly with hypertension (C537095)
..Faye-Petersen Ward Carey syndrome (C537076)
..Hypertension Resistant to Conventional Therapy (C563514)
..Hypertension, Diastolic, Resistance to (C563897)
..Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy (C565359)
..Hypertension, Essential (C562386)
..Hypertension, Malignant (D006974)
..Hypertension, Pregnancy-Induced (D046110) 7
..Hypertension, Renal (D006977) 3
..Hypertensive Retinopathy (D058437)
..Hypomagnesemia, Hypertension, and Hypercholesterolemia, Mitochondrial (C564024)
..Kallikrein hypertension (C537707)
..Masked Hypertension (D059468)
..Osteochondrodysplasia, Rhizomelic, with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension (C563478)
..Tachycardia, Hypertension, Microphthalmia, And Hyperglycinuria (C566880)
..White Coat Hypertension (D059466)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11742
Name:	White Coat Hypertension
Definition:	Phenomenon where BLOOD PRESSURE readings are elevated only when taken in clinical settings.
Alternative IDs:
ParentIDs:	MESH:D006973
TreeNumbers:	C14.907.489.907
Synonyms:	Clinic Hypertension, Isolated \|Hypertension, Isolated Clinic \|Hypertension, White Coat \|Isolated Clinic Hypertension \|Syndrome, White Coat \|White Coat Syndrome
Slim Mappings:	Cardiovascular disease
Reference:	MedGen: D059466 MeSH: D059466 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants