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Diseases

Pulmonary Arterial Hypertension

pulmonary arterial hypertension

Entity Type
Diseases
Relation Groups
2
Relation Preview
16

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Pulmonary Arterial Hypertension
Standard Disease Name
pulmonary arterial hypertension
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D024182
OMIM ID
MTHU009937
UMLS ID
C0949628
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:A condition characterized by the inheritance of a chromosome pair from one parent and no chromosomal copies from the other parent. It results in developmental abnormalities or rare recessive disorders. Examples of uniparental disomy include the Prader-Willi syndrome and Angelman syndrome.|MSH2017_2016_08_12:The presence in a cell of two paired chromosomes from the same parent, with no chromosome of that pair from the other parent. This chromosome composition stems from non-disjunction (NONDISJUNCTION, GENETIC) events during MEIOSIS. The disomy may be composed of both homologous chromosomes from one parent (heterodisomy) or a duplicate of one chromosome (isodisomy).
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

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MCU
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PFKFB3
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6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3