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Diseases

Hereditary Pancreatitis

hereditary pancreatitis

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Hereditary Pancreatitis
Standard Disease Name
hereditary pancreatitis
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
C537262
OMIM ID
276000|167800
UMLS ID
C0238339
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:A disorder characterized by recurrent episodes of pancreatitis that start at a young age. It is caused by mutations in the PRSS1 or SPINK1 genes. Patients are at a high risk of developing pancreatic carcinoma.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
01
BRAF
B-Raf proto-oncogene, serine/threonine kinase
B-Raf proto-oncogene, serine/threonine kinase
05
CYP1B1
cytochrome P450 family 1 subfamily B member 1
cytochrome P450 family 1 subfamily B member 1