DiseaseID 29071
遗传性非息肉病性结直肠癌
Hnec
SNOMEDCT_US_2016_09_01:A rare hepatic tumour that may manifest with abdominal pain or fullness, as well as diarrhoea or weight loss. More than 10% of cases are asymptomatic and in rare cases a carcinoid syndrome may be o
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Disease: 1Symptom: 9Target: 6Links: 15
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 29071
- Core Entity Id
- 121639
- Source Entity Count
- 1
- Preferred Name
- Hnec
- Name Cn
- 遗传性非息肉病性结直肠癌
- Name Pinyin
- Yi Chuan Xing Fei Xi Rou Bing Xing Jie Zhi Chang Ai
- Name En
- Hnec
- 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
- SNOMEDCT_US_2016_09_01:A rare hepatic tumour that may manifest with abdominal pain or fullness, as well as diarrhoea or weight loss. More than 10% of cases are asymptomatic and in rare cases a carcinoid syndrome may be observed. The age of onset is variable. The aetiology is still unknown but it is thought to arise from Kulchitsky cells originating in the neural crest.|SNOMEDCT_US_2016_09_01:A rare hepatic tumor that may manifest with abdominal pain or fullness, as well as diarrhea or weight loss. More than 10% of cases are asymptomatic and in rare cases a carcinoid syndrome may be observed. The age of onset is variable. The etiology is still unknown but it is thought to arise from Kulchitsky cells originating in the neural crest.|NCI2016_02D:An extremely rare, aggressive, high-grade and poorly differentiated carcinoma with neuroendocrine differentiation that arises from the liver.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hnec
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C3273031
Sym Map
SMDE09512
Itcmdb Generated
ITX-DISEASE-DBC432A38E86
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Definition
SNOMEDCT_US_2016_09_01:A rare hepatic tumour that may manifest with abdominal pain or fullness, as well as diarrhoea or weight loss. More than 10% of cases are asymptomatic and in rare cases a carcinoid syndrome may be observed. The age of onset is variable. The aetiology is still unknown but it is thought to arise from Kulchitsky cells originating in the neural crest.|SNOMEDCT_US_2016_09_01:A rare hepatic tumor that may manifest with abdominal pain or fullness, as well as diarrhea or weight loss. More than 10% of cases are asymptomatic and in rare cases a carcinoid syndrome may be observed. The age of onset is variable. The etiology is still unknown but it is thought to arise from Kulchitsky cells originating in the neural crest.|NCI2016_02D:An extremely rare, aggressive, high-grade and poorly differentiated carcinoma with neuroendocrine differentiation that arises from the liver.