Gaucher Disease
An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement.
Year introduced: 2000(1966)
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Tree Number(s): C10.228.140.163.100.435.825.400, C16.320.565.189.435.825.400, C16.320.565.398.641.803.441, C16.320.565.595.554.825.400, C18.452.132.100.435.825.400, C18.452.584.563.641.803.441, C18.452.648.189.435.825.400, C18.452.648.398.641.803.441, C18.452.648.595.554.825.400
MeSH Unique ID: D005776
Entry Terms:
- Disease, Gaucher
- Acid beta-Glucosidase Deficiency Disease
- Acid beta-Glucosidase Deficiency
- Glucocerebrosidase Deficiency
- Deficiencies, Glucocerebrosidase
- Deficiency, Glucocerebrosidase
- Glucocerebrosidase Deficiencies
- Gaucher's Disease
- Disease, Gaucher's
- Gaucher Splenomegaly
- Splenomegaly, Gaucher
- Gaucher Syndrome
- Syndrome, Gaucher
- Gauchers Disease
- Disease, Gauchers
- Diseases, Gauchers
- Gauchers Diseases
- Glucocerebrosidosis
- Glucocerebrosidoses
- Glucosyl Cerebroside Lipidosis
- Cerebroside Lipidoses, Glucosyl
- Cerebroside Lipidosis, Glucosyl
- Glucosyl Cerebroside Lipidoses
- Lipidoses, Glucosyl Cerebroside
- Lipidosis, Glucosyl Cerebroside
- Glucosylceramidase Deficiency
- Glucosylceramide Beta-Glucosidase Deficiency
- Glucosylceramide Lipidosis
- Glucosylceramide Lipidoses
- Lipidoses, Glucosylceramide
- Lipidosis, Glucosylceramide
- Kerasin Histiocytosis
- Histiocytoses, Kerasin
- Histiocytosis, Kerasin
- Kerasin Histiocytoses
- Kerasin Lipoidosis
- Kerasin Lipoidoses
- Lipoidoses, Kerasin
- Lipoidosis, Kerasin
- Kerasin thesaurismosis
- Kerasin thesaurismoses
- thesaurismoses, Kerasin
- thesaurismosis, Kerasin
- Lipoid Histiocytosis (Kerasin Type)
- Histiocytoses, Lipoid (Kerasin Type)
- Histiocytosis, Lipoid (Kerasin Type)
- Lipoid Histiocytoses (Kerasin Type)
- Cerebroside Lipidosis Syndrome
- Cerebroside Lipidosis Syndromes
- Lipidosis Syndrome, Cerebroside
- Lipidosis Syndromes, Cerebroside
- Syndrome, Cerebroside Lipidosis
- Syndromes, Cerebroside Lipidosis
- Glucosylceramide Beta-Glucosidase Deficiency Disease
- Glucocerebrosidase Deficiency Disease
- Deficiency Disease, Glucocerebrosidase
- Deficiency Diseases, Glucocerebrosidase
- Disease, Glucocerebrosidase Deficiency
- Diseases, Glucocerebrosidase Deficiency
- Glucocerebrosidase Deficiency Diseases
- Gaucher Disease, Type 1
- Gaucher Disease, Chronic
- Gaucher Disease, Non-Neuronopathic Form
- Gaucher Disease, Non Neuronopathic Form
- Non-Neuronopathic Gaucher Disease
- Disease, Non-Neuronopathic Gaucher
- Gaucher Disease, Non-Neuronopathic
- Non Neuronopathic Gaucher Disease
- Type 1 Gaucher Disease
- Gaucher Disease Type 1
- Gaucher Disease, Noncerebral Juvenile
- Gaucher Disease, Type I
- Chronic Gaucher Disease
- Disease, Chronic Gaucher
- GBA Deficiency
- Deficiencies, GBA
- Deficiency, GBA
- GBA Deficiencies
- Gaucher Disease, Type 2
- Gaucher Disease, Acute Neuronopathic
- Gaucher Disease, Infantile
- Disease, Infantile Gaucher
- Infantile Gaucher Disease
- Type 2 Gaucher Disease
- Gaucher Disease Type 2
- Gaucher Disease, Infantile Cerebral
- Gaucher Disease, Acute Neuronopathic Type
- Acute Neuronopathic Gaucher Disease
- Gaucher Disease, Type II
- Gaucher Disease, Type 3
- Gaucher Disease, Juvenile
- Disease, Juvenile Gaucher
- Juvenile Gaucher Disease
- Gaucher Disease, Neuronopathic
- Disease, Neuronopathic Gaucher
- Gaucher Disease, Subacute Neuronopathic Form
- Subacute Neuronopathic Gaucher Disease
- Type 3 Gaucher Disease
- Gaucher Disease Type 3
- Gaucher Disease, Chronic Neuronopathic Type
- Gaucher Disease, Juvenile and Adult, Cerebral
- Gaucher Disease, Subacute Neuronopathic Type
- Neuronopathic Gaucher Disease
- Gaucher Disease, Type III
See Also: