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:
Abnormal inflammatory response (HP:0012647)

Parent Node:
Abnormality of bladder morphology (HP:0025487)

Parent Node:
Increased inflammatory response (HP:0012649)

..Starting node
..Urinary bladder inflammation (HP:0100577)

Term ID:

100577

Name:

Urinary bladder inflammation

Synonym:

Cystitis of the urinary bladder; Urinary bladder inflammation

Definition:

Inflammation of the urinary bladder.

Comments:

Reference:

HP:0100577

Genes and Diseases:

Child Nodes:

Sister Nodes:

Cholangitis (HP:0030151)

Chondritis (HP:0100662)

Endocarditis (HP:0100584)

Epididymitis (HP:0000031)

Fasciitis (HP:0100537)

Gastrointestinal inflammation (HP:0004386)

Hepatitis (HP:0012115)

Inflammatory abnormality of the eye (HP:0100533)

Inflammatory abnormality of the skin (HP:0011123)

Lymphadenitis (HP:0002840)

Meningitis (HP:0001287)

Myelitis (HP:0012486)

Myositis (HP:0100614)

Nephritis (HP:0000123)

Optic neuritis (HP:0100653)

Osteomyelitis (HP:0002754)

Otitis media (HP:0000388)

Pancreatitis (HP:0001733)

Panniculitis (HP:0012490)

Periodontitis (HP:0000704)

Pneumonia (HP:0002090)

Prostatitis (HP:0000024)

Serositis (HP:0045073)

Sinusitis (HP:0000246)

Stomatitis (HP:0010280)

Thyroiditis (HP:0100646)

Vaginitis (HP:0030683)

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:0100577	HP:0100577	Urinary bladder inflammation	0	ITGA6 CL E G H	3655	6142	ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia	HP:0040282 - Frequent	79
HP:0100577	HP:0100577	Urinary bladder inflammation	0	ITGB4 CL E G H	3691	6158	ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia	HP:0040282 - Frequent	124

Genes (2) :ITGA6 ITGB4

Diseases (1) :ORPHA:79403

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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