Abnormality of the genitourinary system

Symptom Information:

Symptom ID: HPO:0000119
Synonyms:
Genitourinary abnormality [HPO:0000119]
Genitourinary disease [HPO:0000119]
Genitourinary dysplasia [HPO:0000119]
Genitourinary tract anomalies [HPO:0000119]
Genitourinary tract malformation [HPO:0000119]
Urogenital abnormalities [HPO:0000119]
Urogenital anomalies [HPO:0000119]
Genitourinary tract anomalies [OMIM:Genitourinary tract anomalies]
Urogenital abnormalities [OMIM:Urogenital abnormalities]
Urogenital abnormalities (45%) [OMIM:Urogenital abnormalities (45%)]
Quality:
Cross references:
OMIM: "Genitourinary tract anomalies" [OMIM:Genitourinary tract anomalies]
OMIM: "Urogenital abnormalities" [OMIM:Urogenital abnormalities]
OMIM: "Urogenital abnormalities (45%)" [OMIM:Urogenital abnormalities (45%)]
Is a (Direct Parents):
HPO         Phenotypic abnormality
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
MedDRA:
Database Frequency: 34 / 7739
Resource:

All diseases associated with this symptom:

ADENOMYOSIS (OMIM:600458)
AL amyloidosis (Orphanet:85443)
Adams-Oliver syndrome (Orphanet:974)
Adrenomyodystrophy (Orphanet:977)
Anophthalmia plus syndrome (Orphanet:1104)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 6 (OMIM:605231)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Cardiomyopathy-renal anomalies (Orphanet:90022)
Complete hydatidiform mole (Orphanet:254688)
EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL (OMIM:129840)
Familial intestinal malrotation - facial anomalies (Orphanet:2454)
GALACTORRHEA (OMIM:230300)
GENITOURINARY TRACT ANOMALIES (OMIM:305690)
GONADAL AGENESIS (OMIM:600171)
Hyperlysinemia, type I (OMIM:238700)
Junctional epidermolysis bullosa - pyloric atresia (Orphanet:79403)
LABIA MINORA, INCOMPLETE ADHESION OF (OMIM:149600)
LEUKEMIA, ACUTE MYELOCYTIC, WITH POLYPOSIS COLI AND COLON CANCER (OMIM:246470)
LUJAN-FRYNS SYNDROME (OMIM:309520)
Marden-Walker syndrome (Orphanet:2461)
Mowat-Wilson syndrome (Orphanet:2152)
Nathalie syndrome (Orphanet:2663)
Ovarian hyperstimulation syndrome (Orphanet:64739)
PEYRONIE DISEASE (OMIM:171000)
Primary localized amyloidosis (Orphanet:314709)
Splenogonadal fusion - limb defects - micrognathia (Orphanet:2063)
TMCO1 defect syndrome (Orphanet:228407)
URINARY BLADDER, ATONY OF (OMIM:191800)
VISCERAL STEATOSIS, CONGENITAL (OMIM:228100)
VULVOVAGINITIS, ALLERGIC SEMINAL (OMIM:193450)
Von Voss-Cherstvoy syndrome (Orphanet:3439)