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
fibular collateral ligament bursitis
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 +
tibial muscular dystrophy
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