DiseaseID 29814
Mounier-Kuhn综合征
Mounier Kuhn Syndrome
NCI2016_02D:A rare syndrome of unknown etiology, characterized by marked dilatation of the lumen of the trachea and the main bronchi. It results in bronchiectasis and recurrent lung infections.|MSH2017_2016_08_12:A rare
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Disease: 1Symptom: 2Links: 2
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 29814
- Core Entity Id
- 122382
- Source Entity Count
- 1
- Preferred Name
- Mounier Kuhn Syndrome
- Name Cn
- Mounier-Kuhn综合征
- Name Pinyin
- Mounier-kuhn Zong He Zheng
- Name En
- Mounier Kuhn Syndrome
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- NCI2016_02D:A rare syndrome of unknown etiology, characterized by marked dilatation of the lumen of the trachea and the main bronchi. It results in bronchiectasis and recurrent lung infections.|MSH2017_2016_08_12:A rare and probably congenital condition characterized by great enlargement of the lumen of the trachea and the larger bronchi.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Mounier Kuhn Syndrome
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Omim
275300
Umls
C0040587
Sym Map
SMDE11096
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Definition
NCI2016_02D:A rare syndrome of unknown etiology, characterized by marked dilatation of the lumen of the trachea and the main bronchi. It results in bronchiectasis and recurrent lung infections.|MSH2017_2016_08_12:A rare and probably congenital condition characterized by great enlargement of the lumen of the trachea and the larger bronchi.