Hinman syndrome

General Information (adopted from Orphanet):

Synonyms, Signs: HAS
HS
Hinman-Allen syndrome
Non-neurogenic neurogenic bladder
Occult neuropathic bladder
Number of Symptoms 7
OrphanetNr: 84085
OMIM Id:
ICD-10: N32.8
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset: All ages
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Rare urogenital disease
 -Rare urogenital disease

Symptom Information: Sort by abundance 

1
 (HPO:0000083) Renal insufficiency Occasional [Orphanet] 232 / 7739
2
 (HPO:0000076) Vesicoureteral reflux Frequent [Orphanet] 94 / 7739
3
 (HPO:0011037) Decreased urine output Frequent [Orphanet] 47 / 7739
4
 (HPO:0000010) Recurrent urinary tract infections Frequent [Orphanet] 56 / 7739
5
 (HPO:0000072) Hydroureter Frequent [Orphanet] 146 / 7739
6
 (HPO:0002019) Constipation Frequent [Orphanet] 194 / 7739
7
 (HPO:0002607) Bowel incontinence Frequent [Orphanet] 33 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: