Abnormal localization of kidney

Symptom Information:

Symptom ID: HPO:0100542
Abnormal localisation of kidneys [HPO:0100542]
Cross references:
Is a (Direct Parents):
HPO         Abnormal renal morphology
Is a (Whole tree): HPO:
    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)
Database Frequency: 64 / 7739

All diseases associated with this symptom:

12q14 microdeletion syndrome (Orphanet:94063)
3q29 microdeletion syndrome (Orphanet:65286)
Abruzzo-Erickson syndrome (Orphanet:921)
Acro-pectoro-renal dysplasia (Orphanet:956)
Acro-renal-ocular syndrome (Orphanet:959)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
Baller-Gerold syndrome (Orphanet:1225)
Buschke-Ollendorff syndrome (Orphanet:1306)
C syndrome (Orphanet:1308)
CHARGE syndrome (Orphanet:138)
Cardiocranial syndrome, Pfeiffer type (Orphanet:2872)
Cat-eye syndrome (Orphanet:195)
Caudal regression sequence (Orphanet:3027)
Cenani-Lenz syndrome (Orphanet:3258)
Cloacal exstrophy (Orphanet:93929)
Coffin-Siris syndrome (Orphanet:1465)
Duane retraction syndrome (Orphanet:233)
Ehlers-Danlos syndrome, musculocontractural type (Orphanet:2953)
Epiphyseal dysplasia - hearing loss - dysmorphism (Orphanet:1825)
Faciocardiorenal syndrome (Orphanet:1973)
Fanconi anemia (Orphanet:84)
Femoral-facial syndrome (Orphanet:1988)
Focal dermal hypoplasia (Orphanet:2092)
Goldenhar syndrome (Orphanet:374)
Hennekam syndrome (Orphanet:2136)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Holoprosencephaly - radial heart renal anomalies (Orphanet:3186)
Hypertelorism, Teebi type (Orphanet:1519)
Hypertelorism-microtia-facial clefting syndrome (Orphanet:2213)
Hypoparathyroidism - deafness - renal disease (Orphanet:2237)
Isolated osteopoikilosis (Orphanet:166119)
Juberg-Hayward syndrome (Orphanet:2319)
Kabuki syndrome (Orphanet:2322)
Lathosterolosis (Orphanet:46059)
MURCS association (Orphanet:2578)
Matthew-Wood syndrome (Orphanet:2470)
Mayer-Rokitansky-K├╝ster-Hauser syndrome (Orphanet:3109)
Meacham syndrome (Orphanet:3097)
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus (Orphanet:83473)
Micro syndrome (Orphanet:2510)
Microgastria - limb reduction defect (Orphanet:2538)
Microphthalmia with limb anomalies (Orphanet:1106)
Mosaic trisomy 9 (Orphanet:99776)
Mowat-Wilson syndrome (Orphanet:2152)
Mycophenolate mofetil embryopathy (Orphanet:268249)
Neonatal hemochromatosis (Orphanet:446)
Nephrosis - deafness - urinary tract - digital malformations (Orphanet:2669)
Netherton syndrome (Orphanet:634)
Noonan syndrome with multiple lentigines (Orphanet:500)
Penoscrotal transposition (Orphanet:2842)
Pfeiffer syndrome type 3 (Orphanet:93260)
Renal cysts and diabetes syndrome (Orphanet:93111)
Ruvalcaba syndrome (Orphanet:3121)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Syndactyly - telecanthus - anogenital and renal malformations (Orphanet:140952)
Thrombocytopenia - absent radius (Orphanet:3320)
Toluene embryopathy (Orphanet:1920)
Townes-Brocks syndrome (Orphanet:857)
Trisomy 20p (Orphanet:261318)
Turner syndrome (Orphanet:881)
VACTERL/VATER association (Orphanet:887)
Verloove Vanhorick-Brubakk syndrome (Orphanet:3429)
Williams syndrome (Orphanet:904)