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中文Interstitial Lung Disease 2 (ILD2)
Alias:
Idiopathic Pulmonary Fibrosis
Ipf
Pulmonary Fibrosis, Idiopathic, Susceptibility to
Fibrocystic Pulmonary Dysplasia
Pulmonary Fibrosis, Idiopathic
Idiopathic Pulmonary Fibrosis, Familial
Cryptogenic Fibrosing Alveolitis
Usual Interstitial Pneumonia
Ild2
Uip
Idiopathic Fibrosing Alveolitis, Chronic Form
Idiopathic Pulmonary Fibrosis Familial
Chronic Idiopathic Pulmonary Fibrosis
Ipf - [idiopathic Pulmonary Fibrosis]
Fibrosing Alveolitis, Cryptogenic
Fibrosing Alveolitis Cryptogenic
Interstitial Pneumonitis, Usual
Fibrosis, Pulmonary, Idiopathic
Interstitial Pulmonary Fibrosis
Interstitial Pneumonitis Usual
Fibrosis Idiopathic Pulmonary
Acute Interstitial Pneumonia
Idiopathic Lung Fibrosis
Fibrosing Lung Disease
Pulmonary Fibrosis Nos
Fibrosing Pneumonitis
Hamman-Rich Syndrome
Fibrosing Alveolitis
Hamman-Rich Disease
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间质性肺病2，也被称为特发性肺纤维化，与局部肺纤维化和肺纤维化有关，症状包括运动时气短和干咳。与间质性肺病2有关的重要基因是SFTPA2（表面活性蛋白A2），其相关通路/超级通路包括糖基化疾病和补体级联反应。在该疾病的背景下提到了尼达尼布和非阿片类止痛药。附属组织包括胎盘、脂肪和肺，相关表型为异常肺间质形态和胃食管反流。
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Basic Information
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MALACARDS
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HPO Frequency
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MGI
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IF
