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Differential Diagnosis For Patient/Gauchers disease


List of current finding(s):

Infectious Disorders (Specific Agent)
Salmonella paratyphi
Salmonella osteomyelitis/vertebral
Metabolic, Storage Disorders
Cerebral Gaucher's of infants (acute)
Gaucher's disease
Arteriosclerotic, Vascular, Venous Disorders
Bone necrosis/infarct/osteonecrosis
Splenic infarct
Reference to Organ System
Myelofibrosis, secondary
ACID BETA GLUCOSIDASE DEFIC DIS, Acid beta Glucosidase Deficiency Disease, ACID BETA-GLUCOSIDASE DEFICIENCY, Acid beta-Glucosidase Deficiency Disease, Adult Gaucher disease, ANEMIA SPLENIC FAMILIAL, cerebroside lipidosis, Cerebroside lipidosis syndrome, CEREBROSIDE LIPOIDOSIS (GAUCHERS ADULT FORM), CEREBROSIDE LIPOIDOSIS GAUCHERS ADULT FORM, Chronic adult Gaucher's disease, CHRONIC GAUCHER DIS, Chronic Gaucher Disease, Chronic non-neuropathic Gaucher's disease, Chronic non-neuropathic Gaucher's disease (disorder), familial splenic anemia, GAUCHER DIS, GAUCHER DIS CHRONIC, GAUCHER DIS NON NEURONOPATHIC FORM, GAUCHER DIS TYPE I, Gaucher disease, Gaucher Disease Chronic, Gaucher Disease Non Neuronopathic Form, GAUCHER DISEASE NONCEREBRAL JUVENILE, Gaucher Disease Non-Neuronopathic, Gaucher Disease Non-Neuronopathic Form, Gaucher Disease Type 1, GAUCHER DISEASE TYPE I, Gaucher splenomegaly, Gaucher syndrome, GAUCHERS DIS, Gauchers Disease, Gaucher's disease, Gaucher's disease type I, GBA DEFICIENCY, GD I, Glucocerebrosidase def type I, GLUCOCEREBROSIDASE DEFIC DIS, Glucocerebrosidase deficiency, Glucocerebrosidase Deficiency Disease, Glucocerebrosidase Deficiency Diseases, Glucocerebrosidase deficiency type I, Glucocerebrosidosis, GLUCOSYL CEREBROSIDE LIPIDOSIS, Glucosylceram b-glucosidas def, glucosylceramidase deficiency, Glucosylceramidase deficiency chronic type, GLUCOSYLCERAMIDE BETA GLUCOSIDASE DEFIC DIS, Glucosylceramide Beta Glucosidase Deficiency Disease, Glucosylceramide beta-glucosidase deficiency, Glucosylceramide beta-glucosidase deficiency (disorder), Glucosylceramide Beta-Glucosidase Deficiency Disease, glucosylceramide lipidosis, HISTIOCYTOSIS LIPID KERASIN TYPE, Kerasin histiocytosis, Kerasin lipoidosis, Kerasin thesaurismosis, Kerasin thesaurismosis (disorder), LIPIDOSIS CEREBROSIDE, lipoid histiocytosis (kerasin type), NON NEURONOPATHIC GAUCHER DIS, Non Neuronopathic Gaucher Disease, Non-Neuronopathic Gaucher Disease, Patient, splenomegaly gaucher's, TYPE 1 GAUCHER DIS, Type 1 Gaucher Disease
External Links Related to Patient/Gauchers disease
PubMed (National Library of Medicine)
NGC (National Guideline Clearinghouse)
Medscape (eMedicine)
Harrison's Online (accessmedicine)
NEJM (The New England Journal of Medicine)