Abnormality of the urinary system

Symptom Information:

Symptom ID: HPO:0000079
Synonyms:
Urinary tract abnormalities [HPO:0000079]
Urinary tract abnormality [HPO:0000079]
Urinary tract anomalies [HPO:0000079]
Urinary tract abnormalities [OMIM:Urinary tract abnormalities]
Urinary tract anomalies [OMIM:Urinary tract anomalies]
Quality:
Cross references:
OMIM: "Urinary tract abnormalities" [OMIM:Urinary tract abnormalities]
OMIM: "Urinary tract anomalies" [OMIM:Urinary tract anomalies]
Is a (Direct Parents):
HPO         Abnormality of the genitourinary system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
MedDRA:
Database Frequency: 88 / 7739
Resource:

All diseases associated with this symptom:

3q13 microdeletion syndrome (Orphanet:1621)
Acro-fronto-facio-nasal dysostosis (Orphanet:1784)
Acro-renal-ocular syndrome (Orphanet:959)
Adrenomyodystrophy (Orphanet:977)
Adult-onset autosomal dominant leukodystrophy (Orphanet:99027)
Alkaptonuria (Orphanet:56)
Antley-Bixler syndrome (Orphanet:83)
Atrioventricular defect - blepharophimosis -radial defects (Orphanet:1352)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
BRESEK syndrome (Orphanet:85284)
Blackfan-Diamond anemia (Orphanet:124)
CEREBELLAR VERMIS APLASIA WITH ASSOCIATED FEATURES SUGGESTING SMITH-LEMLI-OPITZSYNDROME AND MECKEL SYNDROME (OMIM:213010)
Camurati-Engelmann disease (Orphanet:1328)
Cocaine embryofetopathy (Orphanet:1911)
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency (Orphanet:90795)
Congenital hydronephrosis (Orphanet:2190)
Congenital primary megaureter (Orphanet:617)
Cystinosis, adult nonnephropathic (OMIM:219750)
Deafness - onychodystrophy (Orphanet:3231)
Desmoid tumor (Orphanet:873)
Dislocation of the hip - dysmorphism (Orphanet:2412)
Distal trisomy 6p (Orphanet:1745)
Dysplastic cortical hyperostosis (Orphanet:2204)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Ellis Van Creveld syndrome (Orphanet:289)
Embryonary disorganization syndrome (Orphanet:1664)
Familial caudal dysgenesis (Orphanet:1768)
Familial hyperaldosteronism type 1 (Orphanet:403)
Familial supernumerary nipples (Orphanet:2456)
Familial visceral myopathy (Orphanet:2604)
Fanconi anemia (Orphanet:84)
Fraser syndrome (Orphanet:2052)
GM1 gangliosidosis (Orphanet:354)
Hemihypertrophy (Orphanet:2128)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hermansky-Pudlak syndrome (Orphanet:79430)
Holoprosencephaly (Orphanet:2162)
Hydrocephaly - low insertion umbilicus (Orphanet:2184)
Iatrogenic botulism (Orphanet:254509)
Isolated Dandy-Walker malformation (Orphanet:217)
Junctional epidermolysis bullosa (Orphanet:305)
Junctional epidermolysis bullosa, non-Herlitz type (Orphanet:89840)
Juvenile amyotrophic lateral sclerosis (Orphanet:300605)
Juvenile primary lateral sclerosis (Orphanet:247604)
Kapur-Toriello syndrome (Orphanet:2328)
Lethal hemolytic anemia - genital anomalies (Orphanet:1046)
Lethal multiple pterygium syndrome (Orphanet:33108)
Lethal restrictive dermopathy (Orphanet:1662)
Limb body wall complex (Orphanet:2369)
MYH9-related thrombocytopenia (Orphanet:182050)
Malignant atrophic papulosis (Orphanet:679)
Marden-Walker syndrome (Orphanet:2461)
Meckel syndrome, type 5 (OMIM:611561)
Megacystis-microcolon-intestinal hypoperistalsis syndrome (Orphanet:2241)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Microphthalmia - microtia - fetal akinesia (Orphanet:2547)
NODULI CUTANEI, MULTIPLE, WITH URINARY TRACT ABNORMALITIES (OMIM:163850)
Nephrosis - deafness - urinary tract - digital malformations (Orphanet:2669)
Non-distal trisomy 10q (Orphanet:1695)
Noonan syndrome (Orphanet:648)
Oculodentodigital dysplasia (Orphanet:2710)
PTEN hamartoma tumor syndrome (Orphanet:306498)
Pelizaeus-Merzbacher disease (Orphanet:702)
Pentasomy X (Orphanet:11)
Peutz-Jeghers syndrome (Orphanet:2869)
Prune belly syndrome (Orphanet:2970)
Recombinant 8 syndrome (Orphanet:96167)
Renal caliceal diverticuli - deafness (Orphanet:2838)
Renal dysplasia - megalocystis - sirenomelia (Orphanet:1850)
Rhombencephalosynapsis (Orphanet:59315)
Sacrococcygeal dysgenesis association (Orphanet:1773)
Scalp-ear-nipple syndrome (Orphanet:2036)
Short rib-polydactyly syndrome (Orphanet:1505)
Silver-Russell syndrome (Orphanet:813)
Sirenomelia (Orphanet:3169)
Spastic paraplegia type 2 (Orphanet:99015)
Spondylocostal dysostosis - anal and genitourinary malformations (Orphanet:94095)
Thrombocytopenia - Robin sequence (Orphanet:3323)
Thrombocytopenia - absent radius (Orphanet:3320)
Thymic-renal-anal-lung dysplasia (Orphanet:3326)
Toriello-Lacassie-Droste syndrome (Orphanet:3339)
Trisomy 12p (Orphanet:1699)
Trisomy 18 (Orphanet:3380)
Williams syndrome (Orphanet:904)
Wolf-Hirschhorn syndrome (Orphanet:280)
Wolfram syndrome 1 (OMIM:222300)
Wolfram syndrome 2 (OMIM:604928)
X-linked immunoneurologic disorder (Orphanet:2571)