DiseaseID 952
肺动脉高压
disease
NCI2016_02D:A rare, progressive, autosomal dominant inherited disorder. It is caused by mutation in the BMPR2 gene in most cases. It is characterized by abnormally high blood pressure in the pulmonary artery, caused by o
Relationship Network
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Disease: 1Experiment: 1Symptom: 7Target: 12Links: 20
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 952
- Core Entity Id
- 1077
- Source Entity Count
- 1
- Preferred Name
- Pulmonary Arterial Hypertension
- Name Cn
- 肺动脉高压
- Name Pinyin
- Fei Dong Mai Gao Ya
- Name En
- Pulmonary Arterial Hypertension
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Cardiovascular Diseases; Respiratory Tract DiseasesRespiratory Tract Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Abnormality of the respiratory system; Abnormality of the cardiovascular system
- Mesh Class Name
- Respiratory Tract DiseasesRespiratory Tract Diseases; Cardiovascular Diseases
- Hpo Class Name
- Abnormality of the respiratory system; Abnormality of the cardiovascular system
- Do Class Name
- disease of anatomical entity
- Disease Definition
- NCI2016_02D:A rare, progressive, autosomal dominant inherited disorder. It is caused by mutation in the BMPR2 gene in most cases. It is characterized by abnormally high blood pressure in the pulmonary artery, caused by obstruction and obliteration of the small pulmonary arteries.|MSH2017_2016_08_12:Familial or idiopathic hypertension in the PULMONARY CIRCULATION which is not secondary to other disease.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Pulmonary Arterial Hypertension
Role
preferred
Name
Familial Primary Pulmonary Hypertension
Role
preferred
Name
Idiopathic Pulmonary Arterial Hypertension
Role
preferred
Name
Idiopathic Pulmonary Hypertension
Role
preferred
Name
Pulmonary Hypertension, Primary, 1
Role
preferred
Name
Pulmonary Hypertension, Primary, 2
Role
preferred
Name
Pulmonary Hypertension, Primary, 3
Role
preferred
Name
Pulmonary Hypertension, Primary, 4
Role
preferred
Name
Pulmonary Hypertension, Primary, Dexfenfluramine Associated
Role
preferred
Name
Pulmonary Hypertension, Primary, Fenfluramine-Associated
Role
preferred
Name
PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED
Role
preferred
Name
PULMONARY VENOOCCLUSIVE DISEASE 1
Role
preferred
Name
Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia
Role
preferred
Name
Increased Blood Pressure In Blood Vessels of Lungs
Role
alias
Name
PAH
Role
alias
Name
PHT
Role
alias
Name
PPH1
Role
alias
Name
PPH1 WITH HHT
Role
alias
Name
PPH2
Role
alias
Name
PPH3
Role
alias
Name
PPH4
Role
alias
Name
Primary Pulmonary Hypertension
Role
alias
Name
Pulmonary Artery Hypertension
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0002092
Herb
HBDIS003685HBDIS007841HBDIS018753HBDIS018754HBDIS020512HBDIS020960HBDIS022118HBDIS022248HBDIS022324HBDIS022325HBDIS022767HBDIS027393
Me Sh
D065627
Omim
178600615342615343615344
Umls
C0152171C0340543C1969342C1969343C2973725C3203102C3714844C3809192C3809198C3888002
Icd10
I27.0
Sym Map
SMDE00069SMDE02144SMDE03633SMDE03781SMDE08650SMDE09767SMDE09768SMDE12582SMDE12595SMDE12596
Do Class
DOID:7
Dis Ge Net
C0152171C0340543C1969342C1969343C2973725C3203102C3714844C3806932C3809192C3809198C3888002C4552070
Umls Sty
T033T047
Hpo Class
HP:0001626HP:0002086
Me Sh Class
C08C14
Tcmbank Disease
1380139481408818787188532243331472318131922471622193739793
Itcmdb Generated
ITX-DISEASE-2A9ACF771450ITX-DISEASE-2BD1B62CA09FITX-DISEASE-3D3942874657ITX-DISEASE-EDC73F57096C
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v1,v2v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
disease
Hpo Class Name
Abnormality of the respiratory system; Abnormality of the cardiovascular system
Do Disease Class
disease of anatomical entity
Hpo Disease Class
Abnormality of the respiratory system; Abnormality of the cardiovascular system
Umls Disease Type
Disease or SyndromeFinding
Disease Definition
NCI2016_02D:A rare, progressive, autosomal dominant inherited disorder. It is caused by mutation in the BMPR2 gene in most cases. It is characterized by abnormally high blood pressure in the pulmonary artery, caused by obstruction and obliteration of the small pulmonary arteries.|MSH2017_2016_08_12:Familial or idiopathic hypertension in the PULMONARY CIRCULATION which is not secondary to other disease.NCI2016_02D:Increased blood pressure in the arteries of the lungs; the etiology is unknown.
Me Sh Disease Class
Cardiovascular Diseases; Respiratory Tract DiseasesRespiratory Tract Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Respiratory Tract DiseasesRespiratory Tract Diseases; Cardiovascular Diseases
Umls Semantic Type Name
Disease or SyndromeFinding