raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:84085

Hinman syndrome

Synonyms: HAS · HS · Hinman-Allen syndrome · Non-neurogenic neurogenic bladder · Occult neuropathic bladder

Type
Disease
Group
Disorder
Age of onset
All ages
Status
active

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enHinman syndromeHAS · HS · Hinman-Allen syndrome · Non-neurogenic neurogenic bladder · Occult neuropathic bladder
frSyndrome de HinmanDyssynergie vésico-sphinctérienne fonctionnelle · HAS · HS · Neuro-vessie non neurogène · Neuro-vessie occulte · Syndrome de Hinman-Allen · Vessie neurogène non neurogène · Vessie neurologique non neurologique et non neurogène
deHinman-SyndromHAS · HS · Hinman-Allen-Syndrom · Nicht-neurogene neurogene Blase · Okkulte neurogene Blase
esSíndrome de HinmanHAS · HS · Síndrome de Hinman-Allen · Vejiga neurogénica no neurogénica · Vejiga neuropática oculta
itSindrome di HinmanVescica neurogena non neurogena · Vescica neuropatica occulta · HAS · HS · Sindrome di Hinman-Allen
nlSyndroom van HinmanHAS · HS · Niet-neurogene overactieve blaas · Occulte neuropathische blaas · Syndroom van Hinman-Allen
ptSíndrome HinmanBexiga neurogénica não neurogénica · HAS · HS · Síndrome Hinman-Allen
plZespół HinmanaHAS · HS · Nieneurogenny-neurogenny pęcherz moczowy · Zespół Hinmana · Zespół Hinmana i Allena
csHinmanův syndromHAS · HS · Hinmanův-Allenův syndrom · Non-neurogenní neurogenní měchýř · Okultní neuropatický měchýř · Hinman-Allenův syndrom
ukСиндром ХінманаHAS · Синдром Хінмана-Алена · HS · Ненейрогенний нейрогенний сечовий міхур · Окультний невропатичний сечовий міхур
zhHinman综合征非神经性神经源性膀胱
trHinman sendromuHS · HAS · Hinman-Allen sendromu · Gizli nöropatik mesane · Nörojenik olmayan nörojenik mesane

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10N32.8NTBTattributedvalidated
ICD-11GC01.YNTBTindexvalidated
MONDO0019395Evalidated
UMLSC1997362Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Point prevalenceUnknown—WorldwideClass onlyNot yet validatedORPHANET

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

16 annotations · validated 2025-10-07
HPOTerm (as annotated by Orphanet)Diagnostic
Frequent (79-30%)
HP:0032465Bladder trabeculation
HP:0040183Encopresis
HP:0000805Enuresis
HP:0000010Recurrent urinary tract infections
HP:0008635Urinary bladder wall hypertrophy
HP:0000020Urinary incontinence
HP:0000016Urinary retention
HP:0000012Urinary urgency
HP:0000076Vesicoureteral reflux
Occasional (29-5%)
HP:0002027Abdominal pain
HP:0002019Constipation
HP:0030157Flank pain
HP:0000126Hydronephrosis
HP:0002018Nausea
HP:0000083Renal insufficiency
Excluded (0%)
HP:0100712Abnormal lumbar spine morphology

Annotation source: 38741815[PMID]

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Sources for this card