Horseshoe kidney
Symptom Information:
Symptom ID: | HPO:0000085 | ||||||||||||||
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) 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) |
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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) |