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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
cystic kidney disease +     
liver disease +     
pancreas disease +     
situs inversus +     
Alcoholic Liver Diseases +   
alpha 1-antitrypsin deficiency  
alveolar echinococcosis  
annular pancreas  
Autosomal Dominant Tubulointerstitial Kidney Disease 1  
Baraitser Rodeck Garner syndrome 
Brachymesomelia Renal Syndrome 
Budd-Chiari syndrome +   
capillariasis 
Carnitine Palmitoyltransferase II Deficiency, Infantile  
Cerebrorenodigital Syndrome with Limb Malformations and Triradiate Acetabula 
clonorchiasis  
COACH syndrome +   
Cyanosis and Hepatic Disease 
cystic echinococcosis  
cystic fibrosis +   
dextrocardia +   
diffuse cystic renal dysplasia  
endocrine pancreas disease +   
exocrine pancreatic insufficiency +   
Focal Nodular Hyperplasia  
Fraser Jequier Chen Syndrome 
Glycogen Storage Disease 0, Liver  
glycogen storage disease IX +   
glycogen storage disease VI  
GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY  
GSD IV, Nonprogressive Hepatic 
Hepatic Granuloma 
Hepatic Insufficiency +   
Hepatic Porphyrias +   
hepatic tuberculosis 
hepatic vascular disease +   
hepatitis +   
Hepatomegaly +   
hepatopulmonary syndrome  
hepatorenal syndrome  
Hypoglossia with Situs Inversus 
immunoglobulin light chain amyloidosis  
Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease 1  
Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease 2  
INTERSTITIAL LUNG AND LIVER DISEASE  
intrahepatic cholestasis +   
Jeune Syndrome Situs Inversus 
Joubert syndrome 1  
Joubert Syndrome 2  
Joubert syndrome 4  
Joubert syndrome 7  
Levocardia 
Liver Abscess +   
liver cirrhosis +   
Liver Fibrocystic Disease and Polydactyly 
liver inflammatory pseudotumor 
Liver Injury +   
Liver Neoplasms +   
Marfanoid Habitus with Situs Inversus 
maturity-onset diabetes of the young type 5  
Meckel Syndrome 12  
Medullary Sponge Kidney +   
mitochondrial DNA depletion syndrome 6  
Multicystic Dysplastic Kidney +   
nephronophthisis +   
neurohypophyseal diabetes insipidus +   
non-congenital cyst of kidney 
opisthorchiasis  
pancreatic agenesis +   
Pancreatic Cyst +   
Pancreatic Fistula  
Pancreatic Lipase Deficiency  
Pancreatic Lipomatosis Duodenal Stenosis 
pancreatic mucinous ductal ectasia 
Pancreatic Neoplasms +   
pancreatic steatorrhea 
pancreatitis +   
paragonimiasis 
Parasitic Liver Diseases +   
Phosphoenolpyruvate Carboxykinase Deficiency +   
polycystic echinococcosis 
polycystic kidney disease +   
polycystic liver disease +   
Pseudo-TORCH Syndrome 2  
Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations  
renal-hepatic-pancreatic dysplasia +   
A physical disorder characterized by pancreatic fibrosis, renal dysplasia and hepatic dysgenesis; it is usual fatal soon after birth. (DO)
retinitis pigmentosa with or without situs inversus  
Retinohepatoendocrinologic Syndrome 
Senior-Loken syndrome +   
serum amyloid A amyloidosis 
Severe Congenital Liver Disease  
Situs Inversus Totalis with Cystic Dysplasia of Kidneys and Pancreas 
steatotic liver disease +   
toxocariasis +   
Trichohepatoneurodevelopmental Syndrome  
tyrosinemia type II  
Ulnar Ray Dysgenesis with Postaxial Polydactyly and Renal Cystic Dysplasia 
ventriculomegaly - cystic kidney disease  
Visceral Heterotaxy 5, Autosomal  
visceral leishmaniasis  
Wilson disease +   
Zellweger syndrome +   

Synonyms
Exact Synonyms: Ivemark's syndrome ;   RHPD
Primary IDs: MESH:C567142
Xrefs: OMIM:PS208540 ;   ORDO:294415
Definition Sources: http://en.wikipedia.org/wiki/Renal-hepatic-pancreatic_dysplasia "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/17605805 "DO" "DO"

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