Enlarged kidneys
Symptom Information:
Symptom ID: | HPO:0000105 | |||||||
Synonyms: |
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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) Enlarged kidneys(HPO:0000105) MedDRA: |
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Database Frequency: | 30 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Acrocephalopolydactyly | (Orphanet:221054) |
Autosomal recessive polycystic kidney disease | (Orphanet:731) |
Beckwith-Wiedemann syndrome | (Orphanet:116) |
Beckwith-Wiedemann syndrome due to 11p15 microdeletion | (Orphanet:231127) |
Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion | (Orphanet:231130) |
Beckwith-Wiedemann syndrome due to CDKN1C mutation | (Orphanet:231120) |
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 | (Orphanet:231117) |
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 | (Orphanet:96193) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Diaphanospondylodysostosis | (Orphanet:66637) |
Glycogen storage disease due to glucose-6-phosphatase deficiency | (Orphanet:364) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
Leprechaunism | (Orphanet:508) |
Nephronophthisis 16 | (OMIM:615382) |
Nephronophthisis 2 | (OMIM:602088) |
Nephronophthisis 3 | (OMIM:604387) |
Nephronophthisis 9 | (OMIM:613824) |
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 | (OMIM:208540) |
RENAL-HEPATIC-PANCREATIC DYSPLASIA 2 | (OMIM:615415) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Renal-hepatic-pancreatic dysplasia | (Orphanet:294415) |
SHORT RIB-POLYDACTYLY SYNDROME, TYPE IIB | (OMIM:615087) |
Senior-Loken syndrome 7 | (OMIM:613615) |
Short-rib thoracic dysplasia 3 with or without polydactyly | (OMIM:613091) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Tyrosinemia type 1 | (Orphanet:882) |
Wilson disease | (Orphanet:905) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |