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Diseases

Warburg Micro Syndrome 4

warburg micro syndrome 4

Entity Type
Diseases
Relation Groups
1
Relation Preview
7

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Warburg Micro Syndrome 4
Standard Disease Name
warburg micro syndrome 4
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
No data
OMIM ID
No data
UMLS ID
C3273031
HPO ID
No data

Description and Extensions

Description
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.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease7 Targets
04
RAB2A
RAB2A, member RAS oncogene family
RAB2A, member RAS oncogene family