| MeSH 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 C18.452.584.687.803.441 C18.452.648.189.435.825.400 C18.452.648.398.641.803.441 C18.452.648.595.554.825.400
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| Concept/Terms |
Gaucher Disease- Gaucher Disease
- Disease, Gaucher
- Glucocerebrosidase Deficiency
- Deficiencies, Glucocerebrosidase
- Deficiency, Glucocerebrosidase
- Glucocerebrosidase Deficiencies
- Glucocerebrosidase Deficiency Disease
- Deficiency Disease, Glucocerebrosidase
- Deficiency Diseases, Glucocerebrosidase
- Disease, Glucocerebrosidase Deficiency
- Diseases, Glucocerebrosidase Deficiency
- Glucocerebrosidase Deficiency Diseases
- 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
- 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)
- Glucosylceramidase Deficiency
- Glucosylceramide Beta-Glucosidase Deficiency Disease
- Acid beta-Glucosidase Deficiency
- Acid beta-Glucosidase Deficiency Disease
- Glucosylceramide Beta-Glucosidase Deficiency
- Cerebroside Lipidosis Syndrome
- Cerebroside Lipidosis Syndromes
- Lipidosis Syndrome, Cerebroside
- Lipidosis Syndromes, Cerebroside
- Syndrome, Cerebroside Lipidosis
- Syndromes, Cerebroside Lipidosis
- Gaucher's Disease
- Disease, Gaucher's
Gaucher Disease, Type 3- Gaucher Disease, Type 3
- Gaucher Disease, Chronic Neuronopathic Type
- Gaucher Disease, Juvenile
- Disease, Juvenile Gaucher
- Juvenile Gaucher Disease
- Gaucher Disease, Juvenile and Adult, Cerebral
- Type 3 Gaucher Disease
- Gaucher Disease, Subacute Neuronopathic Form
- Gaucher Disease, Subacute Neuronopathic Type
- Gaucher Disease, Type III
- Neuronopathic Gaucher Disease
- Subacute Neuronopathic Gaucher Disease
- Gaucher Disease Type 3
- Gaucher Disease, Neuronopathic
- Disease, Neuronopathic Gaucher
Gaucher Disease, Type 1- Gaucher Disease, Type 1
- Gaucher Disease Type 1
- Gaucher Disease, Chronic
- Type 1 Gaucher Disease
- Gaucher Disease, Noncerebral Juvenile
- Gaucher Disease, Type I
- GBA Deficiency
- Deficiencies, GBA
- Deficiency, GBA
- GBA Deficiencies
- Non-Neuronopathic Gaucher Disease
- Disease, Non-Neuronopathic Gaucher
- Gaucher Disease, Non-Neuronopathic
- Non Neuronopathic Gaucher Disease
- Chronic Gaucher Disease
- Disease, Chronic Gaucher
- Gaucher Disease, Non-Neuronopathic Form
- Gaucher Disease, Non Neuronopathic Form
Gaucher Disease, Type 2- Gaucher Disease, Type 2
- Gaucher Disease Type 2
- Gaucher Disease, Acute Neuronopathic
- Type 2 Gaucher Disease
- Gaucher Disease, Infantile
- Disease, Infantile Gaucher
- Gaucher Disease, Infantile Cerebral
- Gaucher Disease, Type II
- Infantile Gaucher Disease
- Acute Neuronopathic Gaucher Disease
- Gaucher Disease, Acute Neuronopathic Type
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