Horseshoe kidney

Symptom Information:

Symptom ID: HPO:0000085
Synonyms:
Horseshoe kidneys [HPO:0000085]
Horseshoe kidney (disorder) [Orphanet:37120]
Horseshoe kidney [Orphanet:37120]
Horseshoe kidney [OMIM:Horseshoe kidney]
Horseshoe kidneys [OMIM:Horseshoe kidneys]
Ectopic/horseshoe/fused kidneys [Orphanet:37120]
Renal fusion anomaly [MedDRA:10068033]
Horseshoe kidney [MedDRA:10068033]
Horseshoe kidney (1 patient) [OMIM:Horseshoe kidney (1 patient)]
Horseshoe kidney (rare) [OMIM:Horseshoe kidney (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: "Horseshoe kidney" [OMIM:Horseshoe kidney]
OMIM: "Horseshoe kidneys" [OMIM:Horseshoe kidneys]
OMIM: "Horseshoe kidney (1 patient)" [OMIM:Horseshoe kidney (1 patient)]
OMIM: "Horseshoe kidney (rare)" [OMIM:Horseshoe kidney (rare)]
OMIM: "Fused kidneys (rare)" [OMIM:Fused kidneys (rare)]
UMLS:C0221353 "Horseshoe 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
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)
                         Horseshoe kidney(HPO:0000085)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
       Renal structural abnormalities and trauma(MedDRA:10038529)
          Horseshoe kidney(HPO:0000085)
Database Frequency: 39 / 7739
Resource:

All diseases associated with this symptom:

ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS (OMIM:201750)
Acro-renal-ocular syndrome (Orphanet:959)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
Bladder exstrophy (Orphanet:93930)
CHARGE syndrome (Orphanet:138)
Craniofacial dyssynostosis (Orphanet:1516)
Currarino triad (Orphanet:1552)
DIAMOND-BLACKFAN ANEMIA 7 (OMIM:612562)
Developmental delay-microcephaly-facial dysmorphism syndrome, Hutterite type (Orphanet:363444)
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, COMPLEMENTATION GROUP P (OMIM:613951)
Faciocardiorenal syndrome (Orphanet:1973)
Fanconi anemia (Orphanet:84)
Focal dermal hypoplasia (Orphanet:2092)
Hennekam syndrome (Orphanet:2136)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Joubert syndrome 18 (OMIM:614815)
Juberg-Hayward syndrome (Orphanet:2319)
Lathosterolosis (Orphanet:46059)
Linear nevus sebaceus syndrome (Orphanet:2612)
MICROPHTHALMIA, SYNDROMIC 9 (OMIM:601186)
Matthew-Wood syndrome (Orphanet:2470)
Microgastria - limb reduction defect (Orphanet:2538)
Mowat-Wilson syndrome (Orphanet:2152)
Neonatal hemochromatosis (Orphanet:446)
Okihiro syndrome (Orphanet:93293)
Orofaciodigital syndrome type 5 (Orphanet:2919)
RENAL AND MULLERIAN DUCT HYPOPLASIA (OMIM:266810)
ROBERTS SYNDROME (OMIM:268300)
Renal coloboma syndrome (Orphanet:1475)
Renal cysts and diabetes syndrome (Orphanet:93111)
Roberts syndrome (Orphanet:3103)
Short stature, Brussels type (Orphanet:2867)
TARP syndrome (Orphanet:2886)
Thrombocytopenia - absent radius (Orphanet:3320)
VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY (OMIM:602200)