Pancreatitis, hereditary

Preferred Label : Pancreatitis, hereditary;

Symbol : PCTT;

CISMeF acronym : HPC; HP; PCTT;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Pancreatitis, chronic; HPC; HP;

Included titles and symbols : Pancreatitis, chronic, susceptibility to; Pancreatitis, calcific; Pancreatitis, chronic, protection against;

Inheritance : Autosomal dominant;

Prefixed ID : #167800;

Details

Origin ID

167800;

UMLS CUI

C0238339;

Automatic exact mappings (from CISMeF team)
- Calcific pancreatitis [ICD-11 Subcategory]
- Calcific pancreatitis [MedDRA LLT]
- Chronic Pancreatitis [NCIt concept]
- Chronic pancreatitis [ICD-11 Category]
- Chronic pancreatitis [HPO term]
- Chronic pancreatitis [MedDRA LLT]
- Chronic pancreatitis [ICD-9 code]
- Chronic pancreatitis (disorder) [SNOMED CT concept]
- DLC1 wt Allele [NCIt concept]
- Familial chronic pancreatitis (disorder) [SNOMED CT concept]
- HP Gene [NCIt concept]
- HPR wt Allele [NCIt concept]
- Haptoglobin [NCIt concept]
- Hematopoietic Stem Cell [NCIt concept]
- Hereditary chronic pancreatitis [ICD-11 Subcategory]
- Hyperplastic Polyp [NCIt concept]
- Hypersensitivity pneumonitis [ORDO Disease]
- Non-syndromic pontocerebellar hypoplasia [ORDO Disease]
- PANCREATITIS CHRONIC [WHO-ART Included Term]
- Pancreatic calcification [HPO term]
- Pancreatic calcification [MedDRA Preferred Term]
- Pancreatitis chronic [MedDRA Preferred Term]
- Pancreatitis relapsing [MedDRA Preferred Term]
- SPINK1 wt Allele [NCIt concept]
- helicobacter pylori [MeSH Descriptor]
- hermanski-pudlak syndrome [MeSH Descriptor]
- hospitals, psychiatric [MeSH Descriptor]
- pancreatitis [MedlinePlus Topic]
- pancreatitis, calcific [MeSH concept]
- pancreatitis, calcific [MeSH Supplementary Concept]
- pancreatitis, chronic [MeSH Descriptor]
- pancreatitis, chronic [MeSH concept]
- pituitary gland [UBERON concept]
- psychiatric hospital [CISMeF Querying Strategy]
- serine peptidase inhibitor Kazal type 1 [ORDO Gene]
- serine peptidase inhibitor Kazal type 1 [HGNC gene]
Currated CISMeF NLP mapping
- Hereditary Pancreatitis [NCIt concept]
- Hereditary chronic pancreatitis [ORDO Disease]
- Hereditary pancreatitis [MedDRA Preferred Term]
- Hereditary pancreatitis [MeSH concept]
- Hereditary pancreatitis (disorder) [SNOMED CT concept]
- hereditary pancreatitis [Disease (Nov.)]
- hereditary pancreatitis [SNOMED Notion]
- hereditary pancreatitis [MeSH Supplementary Concept]
- hereditary pancreatitis [Radlex concept]
DO Cross reference
- pancreatitis [DO Concept]
Genes related to phenotype
- Chymotrypsin C [OMIM gene]
- Cystic fibrosis transmembrane conductance regulator [OMIM gene]
- Protease, serine, 1 [OMIM gene]
- Protease, serine, 2 [OMIM gene]
- Serine protease inhibitor, kazal-type, 1 [OMIM gene]
HPO term(s)
- Abdominal pain [HPO term]
- Abnormal thrombosis [HPO term]
- Autosomal dominant inheritance [HPO term]
- Diabetes mellitus [HPO term]
- Exocrine pancreatic insufficiency [HPO term]
- Fever [HPO term]
- Pancreatic calcification [HPO term]
- Pancreatic insufficiency [HPO term]
- Pancreatic pseudocyst [HPO term]
- Pancreatitis [HPO term]
- Pleural effusion [HPO term]
- Steatorrhea [HPO term]
ORDO concept(s)
- Hereditary chronic pancreatitis [ORDO Disease]
See also inter- (CISMeF)
- chronic pancreatitis [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial chronic pancreatitis (disorder) [SNOMED CT concept]
- Hereditary Pancreatitis [NCIt concept]
- Hereditary chronic pancreatitis [ORDO Disease]
- Hereditary pancreatitis [MedDRA Preferred Term]
- Hereditary pancreatitis [MeSH concept]
- Hereditary pancreatitis (disorder) [SNOMED CT concept]
- hereditary pancreatitis [MeSH Supplementary Concept]
- hereditary pancreatitis [SNOMED Notion]
- hereditary pancreatitis [Radlex concept]
- hereditary pancreatitis [Disease (Nov.)]

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