Renal cyst
Symptom Information:
Symptom ID: | HPO:0000107 | |||||||||||||
Synonyms: |
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Quality: | ||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |