Human Phenotype Ontology

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:
Abnormal joint morphology (HP:0001367)

Parent Node:
Arthritis (HP:0001369)

..Starting node
..Septic arthritis (HP:0003095)

Term ID:

3095

Name:

Septic arthritis

Synonym:

Infected joint

Definition:

Comments:

Reference:

HP:0003095

Genes and Diseases:

Child Nodes:

Sister Nodes:

Arthralgia/arthritis (HP:0005059)

Gout (HP:0001997)

Oligoarthritis (HP:0040313)

Osteoarthritis (HP:0002758)

Rheumatoid arthritis (HP:0001370)

Sterile arthritis (HP:0040310)

Symmetric polyarthritis (HP:0040311)

Temporomandibular arthritis (HP:0040312)

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:0003095	HP:0003095	Septic arthritis	0	BTK CL E G H	695	1133	OMIM:300755	Agammaglobulinemia, X-linked	.	109
HP:0003095	HP:0003095	Septic arthritis	0	BTK CL E G H	695	1133	OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia	.	109
HP:0003095	HP:0003095	Septic arthritis	0	C2ORF69 CL E G H	205327	26799	OMIM:619423	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 53; COXPD53
HP:0003095	HP:0003095	Septic arthritis	0	CFI CL E G H	3426	5394	OMIM:610984	Complement factor I deficiency		57
HP:0003095	HP:0003095	Septic arthritis	0	MTHFD1 CL E G H	4522	7432	OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia	.	5
HP:0003095	HP:0003095	Septic arthritis	0	MYD88 CL E G H	4615	7562	OMIM:612260	MYD88 DEFICIENCY; MYD88D		9
HP:0003095	HP:0003095	Septic arthritis	0	NTRK1 CL E G H	4914	8031	ORPHA:642	Hereditary sensory and autonomic neuropathy type 4	HP:0040283 - Occasional	97

Genes (6) :BTK C2ORF69 CFI MTHFD1 MYD88 NTRK1

Diseases (7) :OMIM:300755 OMIM:307200 OMIM:619423 OMIM:610984 OMIM:617780 OMIM:612260 ORPHA:642

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