Renal cyst

Symptom Information:

Symptom ID: HPO:0000107
Synonyms:
Cystic kidney disease [HPO:0000107]
Cystic kidney disease [OMIM:Cystic kidney disease]
Renal cyst [OMIM:Renal cyst]
Renal cysts [OMIM:Renal cysts]
Renal cysts (1 patient) [OMIM:Renal cysts (1 patient)]
Renal cysts (33%) [OMIM:Renal cysts (33%)]
Renal cysts (in some patients) [OMIM:Renal cysts (in some patients)]
Renal cysts (less common) [OMIM:Renal cysts (less common)]
Renal cyst [MedDRA:10038423]
Single renal cyst [Orphanet:37280]
Simple renal cyst (disorder) [Orphanet:37280]
Simple renal cyst [Orphanet:37280]
Renal cyst (single) [Orphanet:37280]
Quality:
Cross references:
Orphanet:37280 "Renal cyst (single)" [Orphanet:37280]
OMIM: "Cystic kidney disease" [OMIM:Cystic kidney disease]
OMIM: "Renal cyst" [OMIM:Renal cyst]
OMIM: "Renal cysts" [OMIM:Renal cysts]
OMIM: "Renal cysts (1 patient)" [OMIM:Renal cysts (1 patient)]
OMIM: "Renal cysts (33%)" [OMIM:Renal cysts (33%)]
OMIM: "Renal cysts (in some patients)" [OMIM:Renal cysts (in some patients)]
OMIM: "Renal cysts (less common)" [OMIM:Renal cysts (less common)]
UMLS:C0268800 "Simple renal cyst" [Orphanet:37280]
Is a (Direct Parents):
HPO         Abnormal renal morphology
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)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal morphology(HPO:0012210)
                      Renal cyst(HPO:0000107)
MedDRA:
Database Frequency: 126 / 7739
Resource:

All diseases associated with this symptom:

17q12 microdeletion syndrome (Orphanet:261265)
22q11.2 deletion syndrome (Orphanet:567)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2q37 microdeletion syndrome (Orphanet:1001)
46,XX disorder of sex development - anorectal anomalies (Orphanet:2973)
48,XXXY syndrome (Orphanet:96263)
49,XXXXY syndrome (Orphanet:96264)
AXIAL OSTEOMALACIA (OMIM:109130)
Acrocephalosyndactyly (Orphanet:946)
Adult familial nephronophtisis - spastic quadriparesia (Orphanet:2666)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures (Orphanet:73229)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive polycystic kidney disease (Orphanet:731)
BOR syndrome (Orphanet:107)
BRESEK syndrome (Orphanet:85284)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 4 (OMIM:615982)
Beckwith-Wiedemann syndrome due to CDKN1C mutation (Orphanet:231120)
Bifunctional enzyme deficiency (Orphanet:300)
Birt-Hogg-Dube syndrome (Orphanet:122)
Branchio-oculo-facial syndrome (Orphanet:1297)
C syndrome (Orphanet:1308)
Campomelia, Cumming type (Orphanet:1318)
Cantrell pentalogy (Orphanet:1335)
Carnitine palmitoyl transferase II deficiency (Orphanet:157)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
Cerebro-costo-mandibular syndrome (Orphanet:1393)
Congenital nephrotic syndrome, Finnish type (Orphanet:839)
Cornelia de Lange syndrome (Orphanet:199)
Cutis marmorata telangiectatica congenita (Orphanet:1556)
Cystic hamartoma of lung and kidney (Orphanet:2111)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
Diabetic embryopathy (Orphanet:1926)
Double uterus - hemivagina - renal agenesis (Orphanet:3411)
FANCONI ANEMIA, COMPLEMENTATION GROUP O (OMIM:613390)
Fibulo-ulnar hypoplasia - renal anomalies (Orphanet:2256)
Focal dermal hypoplasia (Orphanet:2092)
Fraser syndrome (Orphanet:2052)
Fryns syndrome (Orphanet:2059)
Genito-palato-cardiac syndrome (Orphanet:2075)
HAJDU-CHENEY SYNDROME (OMIM:102500)
Harrod syndrome (Orphanet:2115)
Hepatic fibrosis - renal cysts - intellectual deficit (Orphanet:2031)
Hypoparathyroidism - deafness - renal disease (Orphanet:2237)
Indomethacin embryofetopathy (Orphanet:1909)
Infundibulopelvic stenosis - multicystic kidney (Orphanet:1849)
Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome (Orphanet:369837)
Isolated polycystic liver disease (Orphanet:2924)
Jacobsen syndrome (Orphanet:2308)
Jeune syndrome (Orphanet:474)
Joubert syndrome (Orphanet:475)
Joubert syndrome 1 (OMIM:213300)
Joubert syndrome 14 (OMIM:614424)
Joubert syndrome 16 (OMIM:614465)
Joubert syndrome 2 (OMIM:608091)
Joubert syndrome 20 (OMIM:614970)
Joubert syndrome 21 (OMIM:615636)
Joubert syndrome with hepatic defect (Orphanet:1454)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I (OMIM:210710)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 (OMIM:257300)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 13 (OMIM:615287)
Marden-Walker syndrome (Orphanet:2461)
McKusick-Kaufman syndrome (Orphanet:2473)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 10 (OMIM:614175)
Meckel syndrome, type 2 (OMIM:603194)
Meckel syndrome, type 4 (OMIM:611134)
Meckel syndrome, type 6 (OMIM:612284)
Megacystis-microcolon-intestinal hypoperistalsis syndrome (Orphanet:2241)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Microgastria - limb reduction defect (Orphanet:2538)
Mosaic trisomy 9 (Orphanet:99776)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Multinodular goiter - cystic kidney - polydactyly (Orphanet:2091)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
NPHP3-related Meckel-like syndrome (Orphanet:3032)
Neonatal diabetes - congenital hypothyroidism - congenital glaucoma - hepatic fibrosis - polycystic kidneys (Orphanet:79118)
Nephronophthisis 9 (OMIM:613824)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
Orofaciodigital syndrome type 1 (Orphanet:2750)
PAGOD syndrome (Orphanet:991)
PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER) (OMIM:614883)
PEROXISOME BIOGENESIS DISORDER 1B (OMIM:601539)
PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER) (OMIM:614862)
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) (OMIM:614866)
PMM2-CDG (Orphanet:79318)
Pallister-Hall syndrome (Orphanet:672)
Penoscrotal transposition (Orphanet:2842)
Permanent neonatal diabetes mellitus (Orphanet:99885)
Peters-plus syndrome (Orphanet:709)
Polysyndactyly - cardiac malformation (Orphanet:2934)
Prune belly syndrome (Orphanet:2970)
RENAL DYSPLASIA, CYSTIC, SUSCEPTIBILITY TO (OMIM:601331)
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
Radio-renal syndrome (Orphanet:3015)
Radio-ulnar synostosis - intellectual deficit - hypotonia (Orphanet:3270)
Renal coloboma syndrome (Orphanet:1475)
Renal cysts and diabetes syndrome (Orphanet:93111)
Renal dysplasia - megalocystis - sirenomelia (Orphanet:1850)
Roberts syndrome (Orphanet:3103)
Saldino-Mainzer syndrome (Orphanet:140969)
Senior-Loken syndrome (Orphanet:3156)
Senior-Loken syndrome 5 (OMIM:609254)
Short rib-polydactyly syndrome (Orphanet:1505)
Short-rib thoracic dysplasia 7 with or without polydactyly (OMIM:614091)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Spondylocarpotarsal synostosis (Orphanet:3275)
TUBEROUS SCLEROSIS 1 (OMIM:191100)
TUBEROUS SCLEROSIS 2 (OMIM:613254)
Tetraamelia - multiple malformations (Orphanet:3301)
Tetrasomy 12p (Orphanet:884)
Thomas syndrome (Orphanet:3316)
Thymic-renal-anal-lung dysplasia (Orphanet:3326)
Trisomy 17p (Orphanet:261290)
Trisomy 1q (Orphanet:261344)
Trisomy X (Orphanet:3375)
Tuberous sclerosis (Orphanet:805)
Ulbright-Hodes syndrome (Orphanet:3404)
VACTERL/VATER association (Orphanet:887)
VERHEIJ SYNDROME (OMIM:615583)
Visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay (Orphanet:73246)
Von Hippel-Lindau disease (Orphanet:892)
Zellweger syndrome (Orphanet:912)