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.