Cystic renal dysplasia

Symptom Information:

Symptom ID: HPO:0000800
Synonyms:
Bilateral cystic dysplasia [HPO:0000800]
Renal cystic dysplasia [HPO:0000800]
Renal dysplasia, cystic [HPO:0000800]
Polycystic kidney disease [Orphanet:37200]
Cystic kidney [Orphanet:37200]
Polycystic Kidney Diseases [Orphanet:37200]
Bilateral cystic dysplasia [OMIM:Bilateral cystic dysplasia]
Cystic renal dysplasia [OMIM:Cystic renal dysplasia]
Renal cystic dysplasia [OMIM:Renal cystic dysplasia]
Multicystic kidney/renal dysplasia [Orphanet:37200]
Polycystic kidney [Orphanet:37200]
Kidney polycystic [Orphanet:37200]
Polycystic kidney, unspecified type [Orphanet:37200]
Congenital cystic kidney disease [MedDRA:10010428]
Cystic kidney disease [MedDRA:10010428]
Cystic kidney disease, unspecified [MedDRA:10010428]
Kidney polycystic [MedDRA:10010428]
Medullary cystic disease [MedDRA:10010428]
Medullary cystic kidney [MedDRA:10010428]
Medullary sponge kidney [MedDRA:10010428]
Other specified cystic kidney disease [MedDRA:10010428]
Polycystic kidney [MedDRA:10010428]
Polycystic kidney, autosomal dominant [MedDRA:10010428]
Polycystic kidney, autosomal recessive [MedDRA:10010428]
Polycystic kidney, unspecified type [MedDRA:10010428]
Uraemic medullary cystic disease [MedDRA:10010428]
Nephronophthisis [MedDRA:10010428]
Polycystic hepatorenal disease [MedDRA:10010428]
Cystic kidney [OMIM:Cystic kidney]
Cystic kidneys [OMIM:Cystic kidneys]
Cystic kidneys (rare) [OMIM:Cystic kidneys (rare)]
Cystic renal dysplasia (less common) [OMIM:Cystic renal dysplasia (less common)]
Medullary sponge kidney (rare) [OMIM:Medullary sponge kidney (rare)]
Nephronophthisis (1 patient) [OMIM:Nephronophthisis (1 patient)]
Nephronophthisis (less common) [OMIM:Nephronophthisis (less common)]
Nephronophthisis (rare) [OMIM:Nephronophthisis (rare)]
Polycystic kidney [OMIM:Polycystic kidney]
Renal cystic dysplasia (1 patient) [OMIM:Renal cystic dysplasia (1 patient)]
Quality:
Cross references:
HPO:0000113 "Polycystic kidney dysplasia" [Orphanet:37200]
Orphanet:37200 "Multicystic kidney/renal dysplasia" [Orphanet:37200]
OMIM: "Bilateral cystic dysplasia" [OMIM:Bilateral cystic dysplasia]
OMIM: "Cystic renal dysplasia" [OMIM:Cystic renal dysplasia]
OMIM: "Renal cystic dysplasia" [OMIM:Renal cystic dysplasia]
OMIM: "Cystic kidney" [OMIM:Cystic kidney]
OMIM: "Cystic kidneys" [OMIM:Cystic kidneys]
OMIM: "Cystic kidneys (rare)" [OMIM:Cystic kidneys (rare)]
OMIM: "Cystic renal dysplasia (less common)" [OMIM:Cystic renal dysplasia (less common)]
OMIM: "Medullary sponge kidney (rare)" [OMIM:Medullary sponge kidney (rare)]
OMIM: "Nephronophthisis (1 patient)" [OMIM:Nephronophthisis (1 patient)]
OMIM: "Nephronophthisis (less common)" [OMIM:Nephronophthisis (less common)]
OMIM: "Nephronophthisis (rare)" [OMIM:Nephronophthisis (rare)]
OMIM: "Polycystic kidney" [OMIM:Polycystic kidney]
OMIM: "Renal cystic dysplasia (1 patient)" [OMIM:Renal cystic dysplasia (1 patient)]
UMLS:C0022679 "Cystic kidney" [Orphanet:37200]
UMLS:C0022680 "Polycystic Kidney Diseases" [Orphanet:37200]
Is a (Direct Parents):
Orphanet Multicystic kidney dysplasia
HPO         Renal cyst
MedDRA Renal neoplasm
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)
                         Cystic renal dysplasia(HPO:0000800)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
       Renal neoplasm(HPO:0009726)
          Cystic renal dysplasia(HPO:0000800)
Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104)
    Renal and urinary tract neoplasms malignant and unspecified(MedDRA:10038364)
       Urinary tract neoplasms unspecified malignancy NEC(MedDRA:10046586)
          Renal neoplasm(HPO:0009726)
             Cystic renal dysplasia(HPO:0000800)
Database Frequency: 31 / 7739
Resource:

All diseases associated with this symptom:

Acrocephalopolydactyly (Orphanet:221054)
Autosomal recessive deafness-onychodystrophy syndrome (Orphanet:79500)
Autosomal recessive polycystic kidney disease (Orphanet:731)
Bardet-Biedl syndrome (Orphanet:110)
Branchio-oculo-facial syndrome (Orphanet:1297)
Cleft palate - large ears - small head (Orphanet:2013)
Diaphanospondylodysostosis (Orphanet:66637)
FANCONI ANEMIA, COMPLEMENTATION GROUP O (OMIM:613390)
Fibulo-ulnar hypoplasia - renal anomalies (Orphanet:2256)
Genito-palato-cardiac syndrome (Orphanet:2075)
Joubert syndrome 15 (OMIM:614464)
Joubert syndrome 16 (OMIM:614465)
Joubert syndrome 3 (OMIM:608629)
Lymphangioleiomyomatosis (Orphanet:538)
McKusick-Kaufman syndrome (Orphanet:2473)
Microgastria - limb reduction defect (Orphanet:2538)
Miller-Dieker syndrome (Orphanet:531)
Multicystic renal dysplasia (Orphanet:1851)
POLYCYSTIC KIDNEY DISEASE 1 (OMIM:173900)
POLYCYSTIC KIDNEY, CATARACT, AND CONGENITAL BLINDNESS (OMIM:263100)
Porencephaly-microcephaly-bilateral congenital cataract syndrome (Orphanet:306547)
RENAL DYSPLASIA, CYSTIC, SUSCEPTIBILITY TO (OMIM:601331)
RENAL-HEPATIC-PANCREATIC DYSPLASIA 2 (OMIM:615415)
ROBERTS SYNDROME (OMIM:268300)
Renal coloboma syndrome (Orphanet:1475)
Renal cysts and diabetes syndrome (Orphanet:93111)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Short-rib thoracic dysplasia 1 with or without polydactyly (OMIM:208500)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Tetrasomy 12p (Orphanet:884)