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:
Increased inflammatory response (HP:0012649)

Parent Node:
Abnormality of the peritoneum (HP:0002585)

Parent Node:
Serositis (HP:0045073)

..Starting node
..Peritonitis (HP:0002586)

Term ID:

2586

Name:

Peritonitis

Synonym:

Inflammation of the peritoneum

Definition:

Inflammation of the peritoneum.

Comments:

Reference:

HP:0002586

Genes and Diseases:

Child Nodes:

........

Meconium peritonitis (HP:0030717)

Sister Nodes:

Pericarditis (HP:0001701)

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:0002586	HP:0002586	Peritonitis	0	ACTN4 CL E G H	81	166	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	27
HP:0002586	HP:0002586	Peritonitis	0	ANKFY1 CL E G H	51479	20763	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare
HP:0002586	HP:0002586	Peritonitis	0	ANLN CL E G H	54443	14082	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	6
HP:0002586	HP:0002586	Peritonitis	0	APOL1 CL E G H	8542	618	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	3
HP:0002586	HP:0002586	Peritonitis	0	ARHGAP24 CL E G H	83478	25361	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	4
HP:0002586	HP:0002586	Peritonitis	0	ARHGDIA CL E G H	396	678	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	3
HP:0002586	HP:0002586	Peritonitis	0	BRCA1 CL E G H	672	1100	ORPHA:168829	Primary peritoneal carcinoma	HP:0040281 - Very frequent	5769
HP:0002586	HP:0002586	Peritonitis	0	CALR CL E G H	811	1455	ORPHA:131	Budd-Chiari syndrome	HP:0040283 - Occasional	1
HP:0002586	HP:0002586	Peritonitis	0	CD2AP CL E G H	23607	14258	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	105
HP:0002586	HP:0002586	Peritonitis	0	CDC45 CL E G H	8318	1739	OMIM:617063	Meier-Gorlin syndrome 7		9
HP:0002586	HP:0002586	Peritonitis	0	CFB CL E G H	629	1037	OMIM:615561	COMPLEMENT FACTOR B DEFICIENCY; CFBD		30
HP:0002586	HP:0002586	Peritonitis	0	COL4A3 CL E G H	1285	2204	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	161
HP:0002586	HP:0002586	Peritonitis	0	COQ8B CL E G H	79934	19041	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	35
HP:0002586	HP:0002586	Peritonitis	0	CRB2 CL E G H	286204	18688	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	12
HP:0002586	HP:0002586	Peritonitis	0	DAAM2 CL E G H	23500	18143	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare
HP:0002586	HP:0002586	Peritonitis	0	ELANE CL E G H	1991	3309	ORPHA:2686	Cyclic neutropenia	HP:0040284 - Very rare	79
HP:0002586	HP:0002586	Peritonitis	0	EMP2 CL E G H	2013	3334	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	4
HP:0002586	HP:0002586	Peritonitis	0	F5 CL E G H	2153	3542	ORPHA:131	Budd-Chiari syndrome	HP:0040283 - Occasional	159
HP:0002586	HP:0002586	Peritonitis	0	FOCAD CL E G H	54914	23377	OMIM:619991			3
HP:0002586	HP:0002586	Peritonitis	0	GAPVD1 CL E G H	26130	23375	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare
HP:0002586	HP:0002586	Peritonitis	0	INF2 CL E G H	64423	23791	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	135
HP:0002586	HP:0002586	Peritonitis	0	JAK2 CL E G H	3717	6192	ORPHA:131	Budd-Chiari syndrome	HP:0040283 - Occasional	57
HP:0002586	HP:0002586	Peritonitis	0	MAGI2 CL E G H	9863	18957	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	59
HP:0002586	HP:0002586	Peritonitis	0	MEFV CL E G H	4210	6998	ORPHA:342	Familial Mediterranean fever	HP:0040283 - Occasional	281
HP:0002586	HP:0002586	Peritonitis	0	MEFV CL E G H	4210	6998	OMIM:249100	Familial Mediterranean fever, AR		281
HP:0002586	HP:0002586	Peritonitis	0	MEFV CL E G H	4210	6998	OMIM:134610	FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT		281
HP:0002586	HP:0002586	Peritonitis	0	MVK CL E G H	4598	7530	ORPHA:343	Hyperimmunoglobulinemia D with periodic fever	HP:0040283 - Occasional	150
HP:0002586	HP:0002586	Peritonitis	0	MYH11 CL E G H	4629	7569	OMIM:619351	MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 2; MMIHS2		418
HP:0002586	HP:0002586	Peritonitis	0	MYO1E CL E G H	4643	7599	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	3
HP:0002586	HP:0002586	Peritonitis	0	NPHS1 CL E G H	4868	7908	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	241
HP:0002586	HP:0002586	Peritonitis	0	NPHS2 CL E G H	7827	13394	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	69
HP:0002586	HP:0002586	Peritonitis	0	NUP107 CL E G H	57122	29914	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	5
HP:0002586	HP:0002586	Peritonitis	0	NUP133 CL E G H	55746	18016	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	1
HP:0002586	HP:0002586	Peritonitis	0	NUP160 CL E G H	23279	18017	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare
HP:0002586	HP:0002586	Peritonitis	0	NUP205 CL E G H	23165	18658	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	1
HP:0002586	HP:0002586	Peritonitis	0	NUP37 CL E G H	79023	29929	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare
HP:0002586	HP:0002586	Peritonitis	0	NUP85 CL E G H	79902	8734	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare
HP:0002586	HP:0002586	Peritonitis	0	NUP93 CL E G H	9688	28958	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	5
HP:0002586	HP:0002586	Peritonitis	0	PAX2 CL E G H	5076	8616	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	39
HP:0002586	HP:0002586	Peritonitis	0	PLCE1 CL E G H	51196	17175	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	118
HP:0002586	HP:0002586	Peritonitis	0	PTPRO CL E G H	5800	9678	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	2
HP:0002586	HP:0002586	Peritonitis	0	TBC1D8B CL E G H	54885	24715	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	1
HP:0002586	HP:0002586	Peritonitis	0	TNFRSF1A CL E G H	7132	11916	ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome	HP:0040283 - Occasional	131
HP:0002586	HP:0002586	Peritonitis	0	TRPC6 CL E G H	7225	12338	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	107
HP:0002586	HP:0002586	Peritonitis	0	WT1 CL E G H	7490	12796	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	177
HP:0002586	HP:0030717	Meconium peritonitis	1	CDC45 CL E G H	8318	1739	OMIM:617063	Meier-Gorlin syndrome 7		9

Genes (43) :ACTN4 ANKFY1 ANLN APOL1 ARHGAP24 ARHGDIA BRCA1 CALR CD2AP CDC45 CFB COL4A3 COQ8B CRB2 DAAM2 ELANE EMP2 F5 FOCAD GAPVD1 INF2 JAK2 MAGI2 MEFV MVK MYH11 MYO1E NPHS1 NPHS2 NUP107 NUP133 NUP160 NUP205 NUP37 NUP85 NUP93 PAX2 PLCE1 PTPRO TBC1D8B TNFRSF1A TRPC6 WT1

Diseases (13) :ORPHA:656 ORPHA:168829 ORPHA:131 OMIM:617063 OMIM:615561 ORPHA:2686 OMIM:619991 ORPHA:342 OMIM:249100 OMIM:134610 ORPHA:343 OMIM:619351 ORPHA:32960

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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