Human Phenotype Ontology

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:0045073	HP:0045073	Serositis	0	ACTN4 CL E G H	81	166	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		27
HP:0045073	HP:0045073	Serositis	0	ANKFY1 CL E G H	51479	20763	ORPHA:656	Genetic steroid-resistant nephrotic syndrome
HP:0045073	HP:0045073	Serositis	0	ANLN CL E G H	54443	14082	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		6
HP:0045073	HP:0045073	Serositis	0	APOL1 CL E G H	8542	618	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		3
HP:0045073	HP:0045073	Serositis	0	ARHGAP24 CL E G H	83478	25361	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		4
HP:0045073	HP:0045073	Serositis	0	ARHGDIA CL E G H	396	678	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		3
HP:0045073	HP:0045073	Serositis	0	BRCA1 CL E G H	672	1100	ORPHA:168829	Primary peritoneal carcinoma		5769
HP:0045073	HP:0045073	Serositis	0	C4A CL E G H	720	1323	ORPHA:117	Behçet disease		1
HP:0045073	HP:0045073	Serositis	0	CALR CL E G H	811	1455	ORPHA:131	Budd-Chiari syndrome		1
HP:0045073	HP:0045073	Serositis	0	CCR1 CL E G H	1230	1602	ORPHA:117	Behçet disease
HP:0045073	HP:0045073	Serositis	0	CD2AP CL E G H	23607	14258	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		105
HP:0045073	HP:0045073	Serositis	0	CDC45 CL E G H	8318	1739	OMIM:617063	Meier-Gorlin syndrome 7		9
HP:0045073	HP:0045073	Serositis	0	CFB CL E G H	629	1037	OMIM:615561	COMPLEMENT FACTOR B DEFICIENCY; CFBD		30
HP:0045073	HP:0045073	Serositis	0	COL4A3 CL E G H	1285	2204	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		161
HP:0045073	HP:0045073	Serositis	0	COQ8B CL E G H	79934	19041	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		35
HP:0045073	HP:0045073	Serositis	0	CRB2 CL E G H	286204	18688	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		12
HP:0045073	HP:0045073	Serositis	0	CTLA4 CL E G H	1493	2505	ORPHA:900	Granulomatosis with polyangiitis		10
HP:0045073	HP:0045073	Serositis	0	CTLA4 CL E G H	1493	2505	OMIM:152700	Systemic lupus erythematosus		10
HP:0045073	HP:0045073	Serositis	0	DAAM2 CL E G H	23500	18143	ORPHA:656	Genetic steroid-resistant nephrotic syndrome
HP:0045073	HP:0045073	Serositis	0	DNASE1 CL E G H	1773	2956	OMIM:152700	Systemic lupus erythematosus		3
HP:0045073	HP:0045073	Serositis	0	ELANE CL E G H	1991	3309	ORPHA:2686	Cyclic neutropenia		79
HP:0045073	HP:0045073	Serositis	0	EMP2 CL E G H	2013	3334	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		4
HP:0045073	HP:0045073	Serositis	0	ERAP1 CL E G H	51752	18173	ORPHA:117	Behçet disease		1
HP:0045073	HP:0045073	Serositis	0	F5 CL E G H	2153	3542	ORPHA:131	Budd-Chiari syndrome		159
HP:0045073	HP:0045073	Serositis	0	FAS CL E G H	355	11920	ORPHA:117	Behçet disease		59
HP:0045073	HP:0045073	Serositis	0	FCGR2A CL E G H	2212	3616	OMIM:152700	Systemic lupus erythematosus		6
HP:0045073	HP:0045073	Serositis	0	FCGR2B CL E G H	2213	3618	OMIM:152700	Systemic lupus erythematosus		2
HP:0045073	HP:0045073	Serositis	0	FOCAD CL E G H	54914	23377	OMIM:619991			3
HP:0045073	HP:0045073	Serositis	0	GAPVD1 CL E G H	26130	23375	ORPHA:656	Genetic steroid-resistant nephrotic syndrome
HP:0045073	HP:0045073	Serositis	0	HBA1 CL E G H	3039	4823	ORPHA:163596	Hb Bart's hydrops fetalis		200
HP:0045073	HP:0045073	Serositis	0	HBA2 CL E G H	3040	4824	ORPHA:163596	Hb Bart's hydrops fetalis		88
HP:0045073	HP:0045073	Serositis	0	HLA-B CL E G H	3106	4932	ORPHA:117	Behçet disease		4
HP:0045073	HP:0045073	Serositis	0	HLA-B CL E G H	3106	4932	ORPHA:397	Giant cell arteritis		4
HP:0045073	HP:0045073	Serositis	0	HLA-B CL E G H	3106	4932	ORPHA:29207	Reactive arthritis		4
HP:0045073	HP:0045073	Serositis	0	HLA-DPA1 CL E G H	3113	4938	ORPHA:900	Granulomatosis with polyangiitis
HP:0045073	HP:0045073	Serositis	0	HLA-DPB1 CL E G H	3115	4940	ORPHA:900	Granulomatosis with polyangiitis		1
HP:0045073	HP:0045073	Serositis	0	HLA-DRB1 CL E G H	3123	4948	ORPHA:397	Giant cell arteritis		2
HP:0045073	HP:0045073	Serositis	0	HLA-DRB1 CL E G H	3123	4948	ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		2
HP:0045073	HP:0045073	Serositis	0	IFNGR1 CL E G H	3459	5439	ORPHA:117	Behçet disease		60
HP:0045073	HP:0045073	Serositis	0	IL10 CL E G H	3586	5962	ORPHA:117	Behçet disease		2
HP:0045073	HP:0045073	Serositis	0	IL12A CL E G H	3592	5969	ORPHA:117	Behçet disease
HP:0045073	HP:0045073	Serositis	0	IL12A-AS1 CL E G H	101928376	49094	ORPHA:117	Behçet disease
HP:0045073	HP:0045073	Serositis	0	IL23R CL E G H	149233	19100	ORPHA:117	Behçet disease		1
HP:0045073	HP:0045073	Serositis	0	IL6 CL E G H	3569	6018	ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		2
HP:0045073	HP:0045073	Serositis	0	INF2 CL E G H	64423	23791	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		135
HP:0045073	HP:0045073	Serositis	0	IRF4 CL E G H	3662	6119	ORPHA:3452	Whipple disease		1
HP:0045073	HP:0045073	Serositis	0	JAK2 CL E G H	3717	6192	ORPHA:131	Budd-Chiari syndrome		57
HP:0045073	HP:0045073	Serositis	0	KLRC4 CL E G H	8302	6377	ORPHA:117	Behçet disease
HP:0045073	HP:0045073	Serositis	0	LACC1 CL E G H	144811	26789	ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		1
HP:0045073	HP:0045073	Serositis	0	MAF CL E G H	4094	6776	ORPHA:1272	Aymé-Gripp syndrome		21
HP:0045073	HP:0045073	Serositis	0	MAF CL E G H	4094	6776	OMIM:601088	Ayme-Gripp syndrome		21
HP:0045073	HP:0045073	Serositis	0	MAGI2 CL E G H	9863	18957	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		59
HP:0045073	HP:0045073	Serositis	0	MEFV CL E G H	4210	6998	ORPHA:117	Behçet disease		281
HP:0045073	HP:0045073	Serositis	0	MEFV CL E G H	4210	6998	ORPHA:342	Familial Mediterranean fever		281
HP:0045073	HP:0045073	Serositis	0	MEFV CL E G H	4210	6998	OMIM:249100	Familial Mediterranean fever, AR		281
HP:0045073	HP:0045073	Serositis	0	MEFV CL E G H	4210	6998	OMIM:134610	FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT		281
HP:0045073	HP:0045073	Serositis	0	MIF CL E G H	4282	7097	ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		1
HP:0045073	HP:0045073	Serositis	0	MVK CL E G H	4598	7530	OMIM:260920	Hyper-Igd syndrome		150
HP:0045073	HP:0045073	Serositis	0	MVK CL E G H	4598	7530	ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		150
HP:0045073	HP:0045073	Serositis	0	MYH11 CL E G H	4629	7569	OMIM:619351	MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 2; MMIHS2		418
HP:0045073	HP:0045073	Serositis	0	MYO1E CL E G H	4643	7599	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		3
HP:0045073	HP:0045073	Serositis	0	NOD2 CL E G H	64127	5331	OMIM:186580	Blau syndrome		187
HP:0045073	HP:0045073	Serositis	0	NOD2 CL E G H	64127	5331	ORPHA:90340	Blau syndrome		187
HP:0045073	HP:0045073	Serositis	0	NOD2 CL E G H	64127	5331	OMIM:617321	YAO SYNDROME; YAOS		187
HP:0045073	HP:0045073	Serositis	0	NPHS1 CL E G H	4868	7908	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		241
HP:0045073	HP:0045073	Serositis	0	NPHS2 CL E G H	7827	13394	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		69
HP:0045073	HP:0045073	Serositis	0	NUP107 CL E G H	57122	29914	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		5
HP:0045073	HP:0045073	Serositis	0	NUP133 CL E G H	55746	18016	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		1
HP:0045073	HP:0045073	Serositis	0	NUP160 CL E G H	23279	18017	ORPHA:656	Genetic steroid-resistant nephrotic syndrome
HP:0045073	HP:0045073	Serositis	0	NUP205 CL E G H	23165	18658	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		1
HP:0045073	HP:0045073	Serositis	0	NUP37 CL E G H	79023	29929	ORPHA:656	Genetic steroid-resistant nephrotic syndrome
HP:0045073	HP:0045073	Serositis	0	NUP85 CL E G H	79902	8734	ORPHA:656	Genetic steroid-resistant nephrotic syndrome
HP:0045073	HP:0045073	Serositis	0	NUP93 CL E G H	9688	28958	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		5
HP:0045073	HP:0045073	Serositis	0	P4HA2 CL E G H	8974	8547	ORPHA:397	Giant cell arteritis		3
HP:0045073	HP:0045073	Serositis	0	PAX2 CL E G H	5076	8616	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		39
HP:0045073	HP:0045073	Serositis	0	PLCE1 CL E G H	51196	17175	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		118
HP:0045073	HP:0045073	Serositis	0	PMM2 CL E G H	5373	9115	OMIM:212065	Congenital disorder of glycosylation, type Ia		150
HP:0045073	HP:0045073	Serositis	0	PMM2 CL E G H	5373	9115	ORPHA:79318	PMM2-CDG		150
HP:0045073	HP:0045073	Serositis	0	PRG4 CL E G H	10216	9364	OMIM:208250	Camptodactyly-Arthropathy-Coxa vara-pericarditis syndrome		6
HP:0045073	HP:0045073	Serositis	0	PRG4 CL E G H	10216	9364	ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		6
HP:0045073	HP:0045073	Serositis	0	PRTN3 CL E G H	5657	9495	ORPHA:900	Granulomatosis with polyangiitis
HP:0045073	HP:0045073	Serositis	0	PTPN22 CL E G H	26191	9652	ORPHA:397	Giant cell arteritis		3
HP:0045073	HP:0045073	Serositis	0	PTPN22 CL E G H	26191	9652	ORPHA:900	Granulomatosis with polyangiitis		3
HP:0045073	HP:0045073	Serositis	0	PTPN22 CL E G H	26191	9652	OMIM:152700	Systemic lupus erythematosus		3
HP:0045073	HP:0045073	Serositis	0	PTPRO CL E G H	5800	9678	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		2
HP:0045073	HP:0045073	Serositis	0	RNU7-1 CL E G H	100147744	34033	OMIM:619487	AICARDI-GOUTIERES SYNDROME 9; AGS9
HP:0045073	HP:0045073	Serositis	0	STAT4 CL E G H	6775	11365	ORPHA:117	Behçet disease		2
HP:0045073	HP:0045073	Serositis	0	TBC1D8B CL E G H	54885	24715	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		1
HP:0045073	HP:0045073	Serositis	0	TLR4 CL E G H	7099	11850	ORPHA:117	Behçet disease		3
HP:0045073	HP:0045073	Serositis	0	TNFRSF1A CL E G H	7132	11916	ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		131
HP:0045073	HP:0045073	Serositis	0	TREX1 CL E G H	11277	12269	OMIM:152700	Systemic lupus erythematosus		56
HP:0045073	HP:0045073	Serositis	0	TRPC6 CL E G H	7225	12338	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		107
HP:0045073	HP:0045073	Serositis	0	UBAC2 CL E G H	337867	20486	ORPHA:117	Behçet disease
HP:0045073	HP:0045073	Serositis	0	WT1 CL E G H	7490	12796	ORPHA:656	Genetic steroid-resistant nephrotic syndrome		177
HP:0045073	HP:0002586	Peritonitis	1	ACTN4 CL E G H	81	166	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	27
HP:0045073	HP:0002586	Peritonitis	1	ANKFY1 CL E G H	51479	20763	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare
HP:0045073	HP:0002586	Peritonitis	1	ANLN CL E G H	54443	14082	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	6
HP:0045073	HP:0002586	Peritonitis	1	APOL1 CL E G H	8542	618	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	3
HP:0045073	HP:0002586	Peritonitis	1	ARHGAP24 CL E G H	83478	25361	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	4
HP:0045073	HP:0002586	Peritonitis	1	ARHGDIA CL E G H	396	678	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	3
HP:0045073	HP:0002586	Peritonitis	1	BRCA1 CL E G H	672	1100	ORPHA:168829	Primary peritoneal carcinoma	HP:0040281 - Very frequent	5769
HP:0045073	HP:0001701	Pericarditis	1	C4A CL E G H	720	1323	ORPHA:117	Behçet disease	HP:0040283 - Occasional	1
HP:0045073	HP:0002586	Peritonitis	1	CALR CL E G H	811	1455	ORPHA:131	Budd-Chiari syndrome	HP:0040283 - Occasional	1
HP:0045073	HP:0001701	Pericarditis	1	CCR1 CL E G H	1230	1602	ORPHA:117	Behçet disease	HP:0040283 - Occasional
HP:0045073	HP:0002586	Peritonitis	1	CD2AP CL E G H	23607	14258	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	105
HP:0045073	HP:0002586	Peritonitis	1	CDC45 CL E G H	8318	1739	OMIM:617063	Meier-Gorlin syndrome 7		9
HP:0045073	HP:0002586	Peritonitis	1	CFB CL E G H	629	1037	OMIM:615561	COMPLEMENT FACTOR B DEFICIENCY; CFBD		30
HP:0045073	HP:0002586	Peritonitis	1	COL4A3 CL E G H	1285	2204	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	161
HP:0045073	HP:0002586	Peritonitis	1	COQ8B CL E G H	79934	19041	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	35
HP:0045073	HP:0002586	Peritonitis	1	CRB2 CL E G H	286204	18688	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	12
HP:0045073	HP:0001701	Pericarditis	1	CTLA4 CL E G H	1493	2505	ORPHA:900	Granulomatosis with polyangiitis	HP:0040283 - Occasional	10
HP:0045073	HP:0001701	Pericarditis	1	CTLA4 CL E G H	1493	2505	OMIM:152700	Systemic lupus erythematosus	.	10
HP:0045073	HP:0002586	Peritonitis	1	DAAM2 CL E G H	23500	18143	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare
HP:0045073	HP:0001701	Pericarditis	1	DNASE1 CL E G H	1773	2956	OMIM:152700	Systemic lupus erythematosus	.	3
HP:0045073	HP:0002586	Peritonitis	1	ELANE CL E G H	1991	3309	ORPHA:2686	Cyclic neutropenia	HP:0040284 - Very rare	79
HP:0045073	HP:0002586	Peritonitis	1	EMP2 CL E G H	2013	3334	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	4
HP:0045073	HP:0001701	Pericarditis	1	ERAP1 CL E G H	51752	18173	ORPHA:117	Behçet disease	HP:0040283 - Occasional	1
HP:0045073	HP:0002586	Peritonitis	1	F5 CL E G H	2153	3542	ORPHA:131	Budd-Chiari syndrome	HP:0040283 - Occasional	159
HP:0045073	HP:0001701	Pericarditis	1	FAS CL E G H	355	11920	ORPHA:117	Behçet disease	HP:0040283 - Occasional	59
HP:0045073	HP:0001701	Pericarditis	1	FCGR2A CL E G H	2212	3616	OMIM:152700	Systemic lupus erythematosus	.	6
HP:0045073	HP:0001701	Pericarditis	1	FCGR2B CL E G H	2213	3618	OMIM:152700	Systemic lupus erythematosus	.	2
HP:0045073	HP:0002586	Peritonitis	1	FOCAD CL E G H	54914	23377	OMIM:619991			3
HP:0045073	HP:0002586	Peritonitis	1	GAPVD1 CL E G H	26130	23375	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare
HP:0045073	HP:0001701	Pericarditis	1	HBA1 CL E G H	3039	4823	ORPHA:163596	Hb Bart's hydrops fetalis	HP:0040283 - Occasional	200
HP:0045073	HP:0001701	Pericarditis	1	HBA2 CL E G H	3040	4824	ORPHA:163596	Hb Bart's hydrops fetalis	HP:0040283 - Occasional	88
HP:0045073	HP:0001701	Pericarditis	1	HLA-B CL E G H	3106	4932	ORPHA:117	Behçet disease	HP:0040283 - Occasional	4
HP:0045073	HP:0001701	Pericarditis	1	HLA-B CL E G H	3106	4932	ORPHA:397	Giant cell arteritis	HP:0040283 - Occasional	4
HP:0045073	HP:0001701	Pericarditis	1	HLA-B CL E G H	3106	4932	ORPHA:29207	Reactive arthritis	HP:0040283 - Occasional	4
HP:0045073	HP:0001701	Pericarditis	1	HLA-DPA1 CL E G H	3113	4938	ORPHA:900	Granulomatosis with polyangiitis	HP:0040283 - Occasional
HP:0045073	HP:0001701	Pericarditis	1	HLA-DPB1 CL E G H	3115	4940	ORPHA:900	Granulomatosis with polyangiitis	HP:0040283 - Occasional	1
HP:0045073	HP:0001701	Pericarditis	1	HLA-DRB1 CL E G H	3123	4948	ORPHA:397	Giant cell arteritis	HP:0040283 - Occasional	2
HP:0045073	HP:0001701	Pericarditis	1	HLA-DRB1 CL E G H	3123	4948	ORPHA:85414	Systemic-onset juvenile idiopathic arthritis	HP:0040283 - Occasional	2
HP:0045073	HP:0001701	Pericarditis	1	IFNGR1 CL E G H	3459	5439	ORPHA:117	Behçet disease	HP:0040283 - Occasional	60
HP:0045073	HP:0001701	Pericarditis	1	IL10 CL E G H	3586	5962	ORPHA:117	Behçet disease	HP:0040283 - Occasional	2
HP:0045073	HP:0001701	Pericarditis	1	IL12A CL E G H	3592	5969	ORPHA:117	Behçet disease	HP:0040283 - Occasional
HP:0045073	HP:0001701	Pericarditis	1	IL12A-AS1 CL E G H	101928376	49094	ORPHA:117	Behçet disease	HP:0040283 - Occasional
HP:0045073	HP:0001701	Pericarditis	1	IL23R CL E G H	149233	19100	ORPHA:117	Behçet disease	HP:0040283 - Occasional	1
HP:0045073	HP:0001701	Pericarditis	1	IL6 CL E G H	3569	6018	ORPHA:85414	Systemic-onset juvenile idiopathic arthritis	HP:0040283 - Occasional	2
HP:0045073	HP:0002586	Peritonitis	1	INF2 CL E G H	64423	23791	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	135
HP:0045073	HP:0001701	Pericarditis	1	IRF4 CL E G H	3662	6119	ORPHA:3452	Whipple disease	HP:0040283 - Occasional	1
HP:0045073	HP:0002586	Peritonitis	1	JAK2 CL E G H	3717	6192	ORPHA:131	Budd-Chiari syndrome	HP:0040283 - Occasional	57
HP:0045073	HP:0001701	Pericarditis	1	KLRC4 CL E G H	8302	6377	ORPHA:117	Behçet disease	HP:0040283 - Occasional
HP:0045073	HP:0001701	Pericarditis	1	LACC1 CL E G H	144811	26789	ORPHA:85414	Systemic-onset juvenile idiopathic arthritis	HP:0040283 - Occasional	1
HP:0045073	HP:0001701	Pericarditis	1	MAF CL E G H	4094	6776	ORPHA:1272	Aymé-Gripp syndrome	HP:0040283 - Occasional	21
HP:0045073	HP:0001701	Pericarditis	1	MAF CL E G H	4094	6776	OMIM:601088	Ayme-Gripp syndrome		21
HP:0045073	HP:0002586	Peritonitis	1	MAGI2 CL E G H	9863	18957	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	59
HP:0045073	HP:0001701	Pericarditis	1	MEFV CL E G H	4210	6998	ORPHA:117	Behçet disease	HP:0040283 - Occasional	281
HP:0045073	HP:0002586	Peritonitis	1	MEFV CL E G H	4210	6998	ORPHA:342	Familial Mediterranean fever	HP:0040283 - Occasional	281
HP:0045073	HP:0001701	Pericarditis	1	MEFV CL E G H	4210	6998	ORPHA:342	Familial Mediterranean fever	HP:0040283 - Occasional	281
HP:0045073	HP:0001701	Pericarditis	1	MEFV CL E G H	4210	6998	OMIM:249100	Familial Mediterranean fever, AR		281
HP:0045073	HP:0002586	Peritonitis	1	MEFV CL E G H	4210	6998	OMIM:249100	Familial Mediterranean fever, AR		281
HP:0045073	HP:0002586	Peritonitis	1	MEFV CL E G H	4210	6998	OMIM:134610	FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT		281
HP:0045073	HP:0001701	Pericarditis	1	MIF CL E G H	4282	7097	ORPHA:85414	Systemic-onset juvenile idiopathic arthritis	HP:0040283 - Occasional	1
HP:0045073	HP:0002586	Peritonitis	1	MVK CL E G H	4598	7530	ORPHA:343	Hyperimmunoglobulinemia D with periodic fever	HP:0040283 - Occasional	150
HP:0045073	HP:0002586	Peritonitis	1	MYH11 CL E G H	4629	7569	OMIM:619351	MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 2; MMIHS2		418
HP:0045073	HP:0002586	Peritonitis	1	MYO1E CL E G H	4643	7599	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	3
HP:0045073	HP:0001701	Pericarditis	1	NOD2 CL E G H	64127	5331	ORPHA:90340	Blau syndrome	HP:0040283 - Occasional	187
HP:0045073	HP:0001701	Pericarditis	1	NOD2 CL E G H	64127	5331	OMIM:186580	Blau syndrome		187
HP:0045073	HP:0001701	Pericarditis	1	NOD2 CL E G H	64127	5331	OMIM:617321	YAO SYNDROME; YAOS		187
HP:0045073	HP:0002586	Peritonitis	1	NPHS1 CL E G H	4868	7908	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	241
HP:0045073	HP:0002586	Peritonitis	1	NPHS2 CL E G H	7827	13394	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	69
HP:0045073	HP:0002586	Peritonitis	1	NUP107 CL E G H	57122	29914	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	5
HP:0045073	HP:0002586	Peritonitis	1	NUP133 CL E G H	55746	18016	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	1
HP:0045073	HP:0002586	Peritonitis	1	NUP160 CL E G H	23279	18017	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare
HP:0045073	HP:0002586	Peritonitis	1	NUP205 CL E G H	23165	18658	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	1
HP:0045073	HP:0002586	Peritonitis	1	NUP37 CL E G H	79023	29929	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare
HP:0045073	HP:0002586	Peritonitis	1	NUP85 CL E G H	79902	8734	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare
HP:0045073	HP:0002586	Peritonitis	1	NUP93 CL E G H	9688	28958	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	5
HP:0045073	HP:0001701	Pericarditis	1	P4HA2 CL E G H	8974	8547	ORPHA:397	Giant cell arteritis	HP:0040283 - Occasional	3
HP:0045073	HP:0002586	Peritonitis	1	PAX2 CL E G H	5076	8616	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	39
HP:0045073	HP:0002586	Peritonitis	1	PLCE1 CL E G H	51196	17175	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	118
HP:0045073	HP:0001701	Pericarditis	1	PMM2 CL E G H	5373	9115	OMIM:212065	Congenital disorder of glycosylation, type Ia		150
HP:0045073	HP:0001701	Pericarditis	1	PMM2 CL E G H	5373	9115	ORPHA:79318	PMM2-CDG	HP:0040284 - Very rare	150
HP:0045073	HP:0001701	Pericarditis	1	PRG4 CL E G H	10216	9364	OMIM:208250	Camptodactyly-Arthropathy-Coxa vara-pericarditis syndrome		6
HP:0045073	HP:0001701	Pericarditis	1	PRG4 CL E G H	10216	9364	ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		6
HP:0045073	HP:0001701	Pericarditis	1	PRTN3 CL E G H	5657	9495	ORPHA:900	Granulomatosis with polyangiitis	HP:0040283 - Occasional
HP:0045073	HP:0001701	Pericarditis	1	PTPN22 CL E G H	26191	9652	ORPHA:397	Giant cell arteritis	HP:0040283 - Occasional	3
HP:0045073	HP:0001701	Pericarditis	1	PTPN22 CL E G H	26191	9652	ORPHA:900	Granulomatosis with polyangiitis	HP:0040283 - Occasional	3
HP:0045073	HP:0001701	Pericarditis	1	PTPN22 CL E G H	26191	9652	OMIM:152700	Systemic lupus erythematosus	.	3
HP:0045073	HP:0002586	Peritonitis	1	PTPRO CL E G H	5800	9678	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	2
HP:0045073	HP:0001701	Pericarditis	1	RNU7-1 CL E G H	100147744	34033	OMIM:619487	AICARDI-GOUTIERES SYNDROME 9; AGS9
HP:0045073	HP:0001701	Pericarditis	1	STAT4 CL E G H	6775	11365	ORPHA:117	Behçet disease	HP:0040283 - Occasional	2
HP:0045073	HP:0002586	Peritonitis	1	TBC1D8B CL E G H	54885	24715	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	1
HP:0045073	HP:0001701	Pericarditis	1	TLR4 CL E G H	7099	11850	ORPHA:117	Behçet disease	HP:0040283 - Occasional	3
HP:0045073	HP:0001701	Pericarditis	1	TNFRSF1A CL E G H	7132	11916	ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome	HP:0040281 - Very frequent	131
HP:0045073	HP:0002586	Peritonitis	1	TNFRSF1A CL E G H	7132	11916	ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome	HP:0040283 - Occasional	131
HP:0045073	HP:0001701	Pericarditis	1	TREX1 CL E G H	11277	12269	OMIM:152700	Systemic lupus erythematosus	.	56
HP:0045073	HP:0002586	Peritonitis	1	TRPC6 CL E G H	7225	12338	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	107
HP:0045073	HP:0001701	Pericarditis	1	UBAC2 CL E G H	337867	20486	ORPHA:117	Behçet disease	HP:0040283 - Occasional
HP:0045073	HP:0002586	Peritonitis	1	WT1 CL E G H	7490	12796	ORPHA:656	Genetic steroid-resistant nephrotic syndrome	HP:0040284 - Very rare	177
HP:0045073	HP:0030717	Meconium peritonitis	2	CDC45 CL E G H	8318	1739	OMIM:617063	Meier-Gorlin syndrome 7		9
HP:0045073	HP:0002563	Constrictive pericarditis	2	PRG4 CL E G H	10216	9364	OMIM:208250	Camptodactyly-Arthropathy-Coxa vara-pericarditis syndrome	.	6