Human Phenotype Ontology

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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

Grandparent Node:
Abnormal respiratory system physiology (HP:0002795)

Grandparent Node:
Abnormal vascular physiology (HP:0030163)

Parent Node:
Abnormality of pulmonary circulation (HP:0030875)

..Starting node
..Increased pulmonary capillary wedge pressure (HP:0030876)

Term ID:

30876

Name:

Increased pulmonary capillary wedge pressure

Synonym:

Increased pulmonary arterial wedge pressure; Increased pulmonary artery occlusion pressure

Definition:

Pulmonary capillary wedge pressure (PCWP) above 15mmHg.

Comments:

Reference:

HP:0030876

Genes and Diseases:

Child Nodes:

Sister Nodes:

Elevated pulmonary artery pressure (HP:0004890)

Increased pulmonary vascular resistance (HP:0005317)

Intrapulmonary shunt (HP:0031225)

Pulmonary embolism (HP:0002204)

Pulmonary venous hypertension (HP:0030950)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030876	HP:0030876	Increased pulmonary capillary wedge pressure	0	CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.