Abnormal localization of kidney
Symptom Information:
Symptom ID: | HPO:0100542 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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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) MedDRA: |
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Database Frequency: | 64 / 7739 | ||
Resource: |
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-Küster-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) |