Human Phenotype Ontology

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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 the bladder (HP:0000014)

Parent Node:
Functional abnormality of the bladder (HP:0000009)

..Starting node
..Urinary hesitancy (HP:0000019)

Term ID:

Name:

Urinary hesitancy

Synonym:

Difficulty with flow

Definition:

Difficulty in beginning the process of urination.

Comments:

Reference:

HP:0000019

Genes and Diseases:

Child Nodes:

Sister Nodes:

Detrusor sphincter dyssynergia (HP:0025488)

Dysuria (HP:0100518)

Enuresis (HP:0000805)

Neurogenic bladder (HP:0000011)

Nocturia (HP:0000017)

Pollakisuria (HP:0100515)

Spastic/hyperactive bladder (HP:0005340)

Urinary bladder sphincter dysfunction (HP:0002839)

Urinary incontinence (HP:0000020)

Urinary retention (HP:0000016)

Urinary urgency (HP:0000012)

Vesicoureteral reflux (HP:0000076)

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:0000019	HP:0000019	Urinary hesitancy	0	APRT CL E G H	353	626	ORPHA:976	Adenine phosphoribosyltransferase deficiency	HP:0040283 - Occasional	19
HP:0000019	HP:0000019	Urinary hesitancy	0	HLA-DQB1 CL E G H	3119	4944	OMIM:126200	Multiple sclerosis, susceptibility to	.
HP:0000019	HP:0000019	Urinary hesitancy	0	HLA-DRB1 CL E G H	3123	4948	OMIM:126200	Multiple sclerosis, susceptibility to	.	2
HP:0000019	HP:0000019	Urinary hesitancy	0	PDCD1 CL E G H	5133	8760	OMIM:126200	Multiple sclerosis, susceptibility to	.	1

Genes (4) :APRT HLA-DQB1 HLA-DRB1 PDCD1

Diseases (2) :ORPHA:976 OMIM:126200

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