Human Phenotype Ontology

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Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormality of pancreas physiology (HP:0012091)

Grandparent Node:
Increased inflammatory response (HP:0012649)

Parent Node:
Pancreatitis (HP:0001733)

..Starting node
..Acute pancreatitis (HP:0001735)

Term ID:

1735

Name:

Acute pancreatitis

Synonym:

Acute pancreatic inflammation; Pancreatitis, acute

Definition:

A acute form of pancreatitis.

Comments:

Reference:

HP:0001735

Genes and Diseases:

Child Nodes:

Sister Nodes:

Chronic calcifying pancreatitis (HP:0005236)

Chronic pancreatitis (HP:0006280)

Recurrent pancreatitis (HP:0100027)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001735	HP:0001735	Acute pancreatitis	0	AGPAT2 CL E G H	10555	325	OMIM:608594	Lipodystrophy, congenital generalized, type 1	.	85
HP:0001735	HP:0001735	Acute pancreatitis	0	APOE CL E G H	348	613	ORPHA:412	Dysbetalipoproteinemia	HP:0040283 - Occasional	39
HP:0001735	HP:0001735	Acute pancreatitis	0	BSCL2 CL E G H	26580	15832	OMIM:269700	Lipodystrophy, congenital generalized, type 2	.	105
HP:0001735	HP:0001735	Acute pancreatitis	0	CYBC1 CL E G H	79415	28672	OMIM:618935	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 5; CGD5
HP:0001735	HP:0001735	Acute pancreatitis	0	HMGCL CL E G H	3155	5005	ORPHA:20	3-hydroxy-3-methylglutaric aciduria	HP:0040284 - Very rare	35
HP:0001735	HP:0001735	Acute pancreatitis	0	LMNA CL E G H	4000	6636	OMIM:151660	Lipodystrophy, familial partial, type 2	HP:0040282 - Frequent	645
HP:0001735	HP:0001735	Acute pancreatitis	0	NSMCE2 CL E G H	286053	26513	OMIM:617253	Seckel syndrome 10	.	2
HP:0001735	HP:0001735	Acute pancreatitis	0	RNU7-1 CL E G H	100147744	34033	OMIM:619487	AICARDI-GOUTIERES SYNDROME 9; AGS9

Genes (8) :AGPAT2 APOE BSCL2 CYBC1 HMGCL LMNA NSMCE2 RNU7-1

Diseases (8) :OMIM:608594 ORPHA:412 OMIM:269700 OMIM:618935 ORPHA:20 OMIM:151660 OMIM:617253 OMIM:619487

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.

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