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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
bone disease +     
leishmaniasis +     
liver disease +     
splenic disease +     
Alcoholic Liver Diseases +   
alpha 1-antitrypsin deficiency  
alveolar echinococcosis  
bejel 
bone benign neoplasm +   
Bone Cysts +   
bone development disease +   
bone inflammation disease +   
Bone Malalignment +   
Bone Neoplasms +   
bone remodeling disease +   
bone resorption disease +   
bone structure disease +   
Budd-Chiari syndrome +   
capillariasis 
Carnitine Palmitoyltransferase II Deficiency, Infantile  
Catel Manzke syndrome  
chronic congestive splenomegaly 
clonorchiasis  
Cloverleaf Skull Micromelia Thoracic Dysplasia 
COACH syndrome +   
Coxa Magna 
Coxa Valga 
cutaneous leishmaniasis +   
Cyanosis and Hepatic Disease 
cystic echinococcosis  
Endocrine Bone Diseases +   
Eosinophilic Granuloma  
Expansile Bone Lesions 
Focal Nodular Hyperplasia  
Genu Valgum +   
Genu Varum +   
geroderma osteodysplasticum  
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 
Hamamy Syndrome  
hemangioma of spleen 
Hepatic Granuloma 
Hepatic Insufficiency +   
Hepatic Porphyrias +   
hepatic tuberculosis 
hepatic vascular disease +   
hepatitis +   
Hepatomegaly +   
hepatopulmonary syndrome  
hepatorenal syndrome  
hepatosplenic schistosomiasis  
Ho Kaufman Mcalister Syndrome 
hypersplenism +   
immunoglobulin light chain amyloidosis  
Immunoskeletal Dysplasia with Neurodevelopmental Abnormalities  
Infectious Bone Diseases +   
INTERSTITIAL LUNG AND LIVER DISEASE  
intrahepatic cholestasis +   
ischemic bone disease +   
Joint Dislocations +   
Liver Abscess +   
liver cirrhosis +   
Liver Fibrocystic Disease and Polydactyly 
liver inflammatory pseudotumor 
Liver Injury +   
Liver Neoplasms +   
Metabolic Bone Diseases +   
mitochondrial DNA depletion syndrome 6  
Myoectodermal Gonadal Dysgenesis Syndrome  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND SKELETAL AND BRAIN ABNORMALITIES  
neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures  
opisthorchiasis  
orbital disease +   
osteochondrosis +   
Osteootohepatoenteric Syndrome  
paracoccidioidomycosis +   
paragonimiasis 
Parasitic Liver Diseases +   
Phosphoenolpyruvate Carboxykinase Deficiency +   
Polyasplenia 
polycystic echinococcosis 
polycystic liver disease +   
primary hypertrophic osteoarthropathy +   
proximal symphalangism +   
Pseudo-TORCH Syndrome 2  
Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations  
renal-hepatic-pancreatic dysplasia +   
Retinohepatoendocrinologic Syndrome 
Sclerosing Bone Dysplasia, Mental Retardation 
serum amyloid A amyloidosis 
Severe Congenital Liver Disease  
Slipped Epiphyses +  
sphenoid sinusitis +  
spinal disease +   
splenic abscess 
splenic infarction 
Splenic Neoplasms +   
Splenic Rupture +  
splenic sequestration 
splenic tuberculosis 
steatotic liver disease +   
toxocariasis +   
Tricho-Dento-Osseous Syndrome 1 
Trichohepatoneurodevelopmental Syndrome  
Trochlea of the Humerus, Aplasia of 
tyrosinemia type II  
visceral heterotaxy +   
visceral leishmaniasis  
A leishmaniasis that is the most severe form of the disease caused by protozoan parasites of the Leishmania genus, resulting in the infection of the internal organs such as liver, spleen and bone marrow. The symptoms include fever, weight loss, and an enlarged spleen and liver. (DO)
Wandering Spleen 
Whyte Murphy Syndrome 
Wilson disease +   
yaws +  
Zellweger syndrome +   

Synonyms
Exact Synonyms: black fever ;   infection by visceral leishmaniasis ;   kala azar
Related Synonyms: KAZA1 ;   KAZA2 ;   KAZA3 ;   kala azar, susceptibility to, 1 ;   kala azar, susceptibility to, 2 ;   kala azar, susceptibility to, 3 ;   visceral leishmaniasis, susceptibility to, 1 ;   visceral leishmaniasis, susceptibility to, 3
Primary IDs: MESH:D007898
Alternate IDs: OMIM:608207 ;   OMIM:611381 ;   OMIM:611382
Xrefs: EFO:0005045 ;   ICD10CM:B55.0 ;   ICD9CM:085.0 ;   NCI:C34771 ;   OMIM:PS608207
Definition Sources: http://en.wikipedia.org/wiki/Visceral_leishmaniasis "DO" "DO", http://www.dpd.cdc.gov/dpdx/HTML/Leishmaniasis.htm "DO" "DO"

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