Ectopic kidney

Symptom Information:

Symptom ID: HPO:0000086
Synonyms:
Displaced kidney [HPO:0000086]
Ectopic kidneys [HPO:0000086]
Renal ectopia [HPO:0000086]
Ectopic kidney (disorder) [Orphanet:37120]
Ectopic kidney [Orphanet:37120]
Ectopic kidney [OMIM:Ectopic kidney]
Ectopic kidneys [OMIM:Ectopic kidneys]
Renal ectopia [OMIM:Renal ectopia]
Ectopic/horseshoe/fused kidneys [Orphanet:37120]
Ectopic kidney [MedDRA:10063044]
Dystopic kidney [MedDRA:10063044]
Ectopic kidney (2 patients) [OMIM:Ectopic kidney (2 patients)]
Renal ectopia (rare) [OMIM:Renal ectopia (rare)]
Fused kidneys [Orphanet:37120]
Fusion of kidneys (disorder) [Orphanet:37120]
Congenital fusion of kidneys [Orphanet:37120]
Fused kidneys (rare) [OMIM:Fused kidneys (rare)]
Quality:
Cross references:
Orphanet:37120 "Ectopic/horseshoe/fused kidneys" [Orphanet:37120]
OMIM: "Ectopic kidney" [OMIM:Ectopic kidney]
OMIM: "Ectopic kidneys" [OMIM:Ectopic kidneys]
OMIM: "Renal ectopia" [OMIM:Renal ectopia]
OMIM: "Ectopic kidney (2 patients)" [OMIM:Ectopic kidney (2 patients)]
OMIM: "Renal ectopia (rare)" [OMIM:Renal ectopia (rare)]
OMIM: "Fused kidneys (rare)" [OMIM:Fused kidneys (rare)]
UMLS:C0238207 "Ectopic kidney" [Orphanet:37120]
UMLS:C0266305 "Congenital fusion of kidneys" [Orphanet:37120]
Is a (Direct Parents):
MedDRA Renal structural abnormalities and trauma
HPO         Abnormal localization of kidney
Orphanet Horseshoe kidney
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)
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)