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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
非罕见病
Pneumonia
Alias:
Acute Pneumonia
Human Metapneumovirus Infection Resulting in Pneumonia
Bronchopneumonia Due to Streptococcus Pneumoniae
Bronchopneumonia Due to Hemophilus Influenzae
Pyemic Pneumococcal Embolism with Pneumonia
Streptococcus Pneumoniae Lobar Pneumonia
Pneumonia Due to Streptococcus, Group B
Pneumonia Due to Hemophilus Influenzae
Haemophilus Influenzae Lobar Pneumonia
Pneumonia Due to Chlamydia Pneumoniae
Bronchopneumonia Due to H. Influenzae
Bronchopneumonia Due to S. Pneumoniae
Pneumonia Respiratory Syncytial Viral
Streptococcal Pneumoniae Pneumonia
Staphylococcal Purulent Pneumonia
Escherichia Coli Lobar Pneumonia
Staphylococcal Double Pneumonia
Staphylococcal Bronchopneumonia
Group B Streptococcal Pneumonia
Human Metapneumovirus Pneumonia
Pneumonia Due to H. Influenzae
Acute Staphylococcal Pneumonia
Staphylococcal Lobar Pneumonia
Parainfluenza Viral Pneumonia
Parainfluenza Virus Pneumonia
Interstitial Lobar Pneumonia
Pneumococcal Lobar Pneumonia
Pseudomonas Lobar Pneumonia
Pneumonia Due to Chlamydia
Adenovirus Viral Pneumonia
Pneumonia Due to E. Coli
Staphylococcal Pneumonia
Staphylococcus Pneumonia
Parainfluenzal Pneumonia
Pneumocystis Pneumonia
Pneumonia, Unspecified
Pneumococcal Pneumonia
Pneumococcus Pneumonia
Plasma Cells Pneumonia
Orthostatic Pneumonia
Chronic Pneumonia Nos
Pseudomonal Pneumonia
Pseudomonas Pneumonia
Infectious Pneumonia
Multifocal Pneumonia
Adenovirus Pneumonia
Adenoviral Pneumonia
Lobar Pneumonia Nos
Atypical Pneumonia
Purulent Pneumonia
Passive Pneumonia
Pn - [pneumonia]
Pneumonia Nos
Rsv Pneumonia
Pneumonias
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基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
肺炎,又称为急性肺炎,与隐源性组织化肺炎和肺炎球菌病有关,症状包括咳嗽、发热和咯血。与肺炎相关的基因包括SKAP1-AS1(SKAP1反义RNA1),其相关通路/超级通路包括ERK信号通路和先天免疫系统。在该疾病的背景下提到了卡泊芬净和碳酸钙。相关组织包括肺和骨髓,相关表型包括shRNA丰度增加(Z-score>2)和稳态/代谢。
Related ID:
MALACARDS:PNM007
MESH:D011014
ICD11:1024154490/other
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
未知
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69
752
3
PNM007
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
#
Gene
Function
Score
Mutations
No data available
Related Drugs
Name
CAS Number
Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
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Publications
No data available
References Literature
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No Data Found!
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