Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Progressive pulmonary hypertension |
Is a |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
|
Solitary pulmonary hypertension |
Is a |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
|
Pulmonary hypertensive arterial disease (disorder) |
Is a |
False |
Pulmonary hypertension |
Inferred relationship |
Some |
|
Pulmonary hypertensive venous disease |
Is a |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
|
Eisenmengers syndrom |
Is a |
False |
Pulmonary hypertension |
Inferred relationship |
Some |
|
Episodic pulmonary hypertension |
Is a |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
|
Secondary pulmonary hypertension |
Is a |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
|
pulmonal hypertension associeret med septumdefekt/shunt |
Is a |
False |
Pulmonary hypertension |
Inferred relationship |
Some |
|
Persistent pulmonary hypertension of the newborn |
Is a |
False |
Pulmonary hypertension |
Inferred relationship |
Some |
|
højresidig hjerteinsufficiens forårsaget af pulmonal hypertension |
Due to |
False |
Pulmonary hypertension |
Inferred relationship |
Some |
1 |
Portopulmonary hypertension (disorder) |
Is a |
False |
Pulmonary hypertension |
Inferred relationship |
Some |
|
Post-capillary pulmonary hypertension |
Is a |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
|
Precapillary pulmonary hypertension |
Is a |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
|
A rare genetic mitochondrial disease with characteristics of early-onset progressive renal failure, manifesting with hyperuricaemia, hyponatraemia, hypomagnesaemia, hypochloraemic metabolic alkalosis, elevated BUN and polyuria, associated with systemic manifestations which include pulmonary hypertension, failure to thrive, global developmental delay, hypotonia and ventricular hypertrophy. Additional features include prematurity, elevated serum lactate, diabetes mellitus and in some pancytopenia. Caused by homozygous mutation in the SARS2 gene, which encodes mitochondrial seryl-tRNA synthetase on chromosome 19q13.2. |
Is a |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
|
Mild pulmonary hypertension |
Is a |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
|
Moderate pulmonary hypertension |
Is a |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
|
Severe pulmonary hypertension |
Is a |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
|
Pulmonary hypertension suspected (situation) |
Associated finding |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
1 |
Pulmonary hypertension due to developmental abnormality (disorder) |
Is a |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
|
Pulmonary hypertension due to pulmonary disease with mixed restrictive and obstructive patterns |
Is a |
False |
Pulmonary hypertension |
Inferred relationship |
Some |
|
Ayerza's syndrome |
Due to |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
2 |
Cor pulmonale |
Due to |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
1 |
Chronic cor pulmonale |
Due to |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
3 |
Acute cor pulmonale |
Due to |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
3 |
Acute cor pulmonale co-occurrent and due to saddle embolus of pulmonary artery (disorder) |
Due to |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
2 |
Acute cor pulmonale due to septic pulmonary embolism |
Due to |
True |
Pulmonary hypertension |
Inferred relationship |
Some |
5 |