Enlarged kidneys

Symptom Information:

Symptom ID: HPO:0000105
Synonyms:
Large kidneys [HPO:0000105]
Nephromegaly [HPO:0000105]
Renal enlargement [HPO:0000105]
Enlarged kidneys [OMIM:Enlarged kidneys]
Large kidneys [OMIM:Large kidneys]
Nephromegaly [OMIM:Nephromegaly]
Renal enlargement [OMIM:Renal enlargement]
Quality:
Cross references:
OMIM: "Enlarged kidneys" [OMIM:Enlarged kidneys]
OMIM: "Large kidneys" [OMIM:Large kidneys]
OMIM: "Nephromegaly" [OMIM:Nephromegaly]
OMIM: "Renal enlargement" [OMIM:Renal enlargement]
Is a (Direct Parents):
HPO         Abnormal renal morphology
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:
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)