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遗传性肺动脉高压

Heritable pulmonary arterial hypertension

ORPHA:275777疾病亚型

定义

遗传性肺动脉高压(HPAH)是肺动脉高压(PAH)的一种形式,由PAH易感基因突变或家族背景所致。HPAH的特点是肺动脉阻力升高导致右心衰竭。HPAH是进行性的,具有潜在的致命性。

别名

遗传性肺动脉高压

基本事实

遗传方式
常染色体显性、常染色体隐性
发病年龄
各年龄段
患病率
<1 / 1 000 000(Europe)

相关基因 11

基因名称关联类型
ACVRL1activin A receptor like type 1Candidate gene tested in
BMPR2bone morphogenetic protein receptor type 2Disease-causing germline mutation(s) (loss of function) in
TBX4T-box transcription factor 4Disease-causing germline mutation(s) in
ENGendoglinCandidate gene tested in
CAV1caveolin 1Disease-causing germline mutation(s) in
SMAD9SMAD family member 9Disease-causing germline mutation(s) in
SOX17SRY-box transcription factor 17Major susceptibility factor in
KCNK3potassium two pore domain channel subfamily K member 3Disease-causing germline mutation(s) (loss of function) in
GDF2growth differentiation factor 2Disease-causing germline mutation(s) in
EIF2AK4eukaryotic translation initiation factor 2 alpha kinase 4Disease-causing germline mutation(s) (loss of function) in
ATP13A3ATPase 13A3Disease-causing germline mutation(s) in

外部标识与链接

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本页数据来源

  • 疾病定义、同义词、基因、表型、流行病学:Orphanet(CC BY 4.0)
  • 中文病名:Orphanet 中文包,冻结于 2020-06-01
  • 表型中文标签:HPO 简体中文翻译(CHPO 上游成果)