Hinman syndrome
MONDO:0019395Mondo
Findings
No curated finding names Hinman syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Hinman syndrome (HS) or non-neurogenic neurogenic bladder is a voiding dysfunction of the bladder of neuropsychological origin that is characterized by functional bladder outlet obstruction in the absence of neurologic deficits.
Definition from the Mondo Disease Ontology (MONDO:0019395), read 2026-09-29. CC BY 4.0.
Features
15 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Bladder trabeculationHPOHP:0032465
- Frequent (30% to 79% of cases)
- EncopresisHPOHP:0040183
- Frequent (30% to 79% of cases)
- EnuresisHPOHP:0000805
- Frequent (30% to 79% of cases)
- Recurrent urinary tract infectionsHPOHP:0000010
- Frequent (30% to 79% of cases)
- Urinary bladder wall hypertrophyHPOHP:0008635
- Frequent (30% to 79% of cases)
- Urinary incontinenceHPOHP:0000020
- Frequent (30% to 79% of cases)
- Urinary retentionHPOHP:0000016
- Frequent (30% to 79% of cases)
- Urinary urgencyHPOHP:0000012
- Frequent (30% to 79% of cases)
- Vesicoureteral refluxHPOHP:0000076
- Frequent (30% to 79% of cases)
- Abdominal painHPOHP:0002027
- Occasional (5% to 29% of cases)
- ConstipationHPOHP:0002019
- Occasional (5% to 29% of cases)
- Flank painHPOHP:0030157
- Occasional (5% to 29% of cases)
Reported absent (1)
- Abnormal lumbar spine morphologyHPOHP:0100712
Show the remaining 3
- HydronephrosisHPOHP:0000126
- Occasional (5% to 29% of cases)
- NauseaHPOHP:0002018
- Occasional (5% to 29% of cases)
- Renal insufficiencyHPOHP:0000083
- Occasional (5% to 29% of cases)
Where it sits
- A kind of
Other names
5 names
Resolves to: Hinman syndrome
- Also called
- HASHinman-Allen syndromeHSnon-neurogenic neurogenic bladderoccult neuropathic bladder