Ectopic kidney
Symptom Information:
Symptom ID: | HPO:0000086 | |||||||||||||||||
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) Abnormal localization of kidney(HPO:0100542) Ectopic kidney(HPO:0000086) MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Renal structural abnormalities and trauma(MedDRA:10038529) Ectopic kidney(HPO:0000086) |
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Database Frequency: | 29 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
CORNELIA DE LANGE SYNDROME 1 | (OMIM:122470) |
Cerebro-costo-mandibular syndrome | (Orphanet:1393) |
Coffin-Siris syndrome | (Orphanet:1465) |
Combined immunodeficiency with facio-oculo-skeletal anomalies | (Orphanet:221139) |
Cornelia de Lange syndrome | (Orphanet:199) |
DIAMOND-BLACKFAN ANEMIA 10 | (OMIM:613309) |
FANCONI ANEMIA, COMPLEMENTATION GROUP A | (OMIM:227650) |
FANCONI ANEMIA, COMPLEMENTATION GROUP C | (OMIM:227645) |
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 | (OMIM:227646) |
FANCONI ANEMIA, COMPLEMENTATION GROUP E | (OMIM:600901) |
Fanconi anemia | (Orphanet:84) |
Goldenhar syndrome | (Orphanet:374) |
Hennekam syndrome | (Orphanet:2136) |
Hypertelorism-microtia-facial clefting syndrome | (Orphanet:2213) |
MURCS association | (Orphanet:2578) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Neonatal hemochromatosis | (Orphanet:446) |
Orofaciodigital syndrome type 5 | (Orphanet:2919) |
PELVIC LIPOMATOSIS WITH CROSSED RENAL ECTOPIA | (OMIM:169545) |
Pallister-Hall syndrome | (Orphanet:672) |
Porencephaly-microcephaly-bilateral congenital cataract syndrome | (Orphanet:306547) |
Radio-renal syndrome | (Orphanet:3015) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
SCHIZOPHRENIA 1 | (OMIM:181510) |
SECKEL SYNDROME 2 | (OMIM:606744) |
SECKEL SYNDROME 8 | (OMIM:615807) |
VACTERL/VATER association | (Orphanet:887) |
VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY | (OMIM:602200) |