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Term:
Parent Terms Term With Siblings Child Terms
Amniotic Band Syndrome +  
asphyxia neonatorum +   
benign neonatal seizures +   
Birth Injuries +   
Caffey disease +   
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal  
cholesterol ester storage disease +   
Colic 
Congenital Hyperinsulinism +   
congenital nystagmus +   
congenital syphilis +  
congenital toxoplasmosis 
Cutis Laxa-Marfanoid Syndrome 
cystic fibrosis +   
fetal erythroblastosis +   
hydrophthalmos +   
Hyperglycinemia, Transient Neonatal 
Hyperparathyroidism, Neonatal Severe Primary  
ichthyosis +   
Infantile Hypercalcemia +   
meconium aspiration syndrome  
Meconium Ileus  
Mobius syndrome +   
neonatal abstinence syndrome 
Neonatal Alloimmune Thrombocytopenia  
neonatal anemia +   
neonatal diabetes mellitus +   
Neonatal Hyperbilirubinemia +   
Neonatal Hypoglycemia, Simulating Foetopathia Diabetica 
Neonatal Inflammatory Skin and Bowel Disease +   
Neonatal Pulmonary Hypertension  
Neonatal Sepsis 
ophthalmia neonatorum 
persistent fetal circulation syndrome  
Posttransfusion Purpura  
Premature Infant Diseases +   
Rothmund-Thomson syndrome +   
Sclerema Neonatorum 
severe combined immunodeficiency +   
thanatophoric dysplasia +   
transient neonatal thrombocytopenia 
umbilical hernia +   
vitamin K deficiency bleeding  
Wolman disease +   
The severe infantile form of inherited lysosomal lipid storage diseases due to deficiency of acid lipase (STEROL ESTERASE). It is characterized by the accumulation of neutral lipids, particularly CHOLESTEROL ESTERS in leukocytes, fibroblasts, and hepatocytes. It is also known as Wolman's xanthomatosis and is an allelic variant of CHOLESTEROL ESTER STORAGE DISEASE.

Synonyms
Exact Synonyms: Acid Lipase Deficiency ;   Familial Xanthomatoses ;   Familial Xanthomatosis ;   Liposomal Acid Lipase Deficiency, Wolman Type ;   Wolman xanthomatosis ;   Wolman's Disease ;   Wolman's Xanthomatosis ;   Wolman's or triglyceride storage type III disease ;   Wolmans disease ;   Wolmans xanthomatosis ;   acid cholesteryl ester hydrolase deficiency, Wolman type ;   acid esterase deficiency
Primary IDs: MESH:D015223
Alternate IDs: RDO:0000244
Xrefs: GARD:7899
Definition Sources: MESH:D015223

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