Multicystic kidney dysplasia
Symptom Information:
Symptom ID: | HPO:0000003 | |||||||||||||||
Synonyms: |
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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) Multicystic kidney dysplasia(HPO:0000003) MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Renal structural abnormalities and trauma(MedDRA:10038529) Multicystic kidney dysplasia(HPO:0000003) |
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Database Frequency: | 17 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
17q12 microdeletion syndrome | (Orphanet:261265) |
BRESEK syndrome | (Orphanet:85284) |
Bardet-Biedl syndrome | (Orphanet:110) |
Genitopatellar syndrome | (Orphanet:85201) |
Goldenhar syndrome | (Orphanet:374) |
Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
Infundibulopelvic stenosis - multicystic kidney | (Orphanet:1849) |
Lymphangioleiomyomatosis | (Orphanet:538) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 | (OMIM:236670) |
Meckel syndrome, type 3 | (OMIM:607361) |
Meckel syndrome, type 9 | (OMIM:614209) |
Multicystic renal dysplasia | (Orphanet:1851) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
Renal coloboma syndrome | (Orphanet:1475) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Simpson-Golabi-Behmel syndrome type 2 | (Orphanet:79022) |
Townes-Brocks syndrome | (Orphanet:857) |