Cystic renal dysplasia
Symptom Information:
Symptom ID: | HPO:0000800 | ||||||||||||||||||||||||||||||||||||||
Synonyms: |
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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) 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) |
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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) |