Gaucher Disease


Acid beta-Glucosidase Deficiency

Acid beta-Glucosidase Deficiency Disease

Acute Neuronopathic Gaucher Disease

Cerebroside Lipidoses, Glucosyl

Cerebroside Lipidosis Syndrome

Cerebroside Lipidosis Syndromes

Cerebroside Lipidosis, Glucosyl

Chronic Gaucher Disease

Deficiencies, GBA

Deficiencies, Glucocerebrosidase

Deficiency Disease, Glucocerebrosidase

Deficiency Diseases, Glucocerebrosidase

Deficiency, GBA

Deficiency, Glucocerebrosidase

Disease, Chronic Gaucher

Disease, Gaucher

Disease, Gaucher's

Disease, Gauchers

Disease, Glucocerebrosidase Deficiency

Disease, Infantile Gaucher

Disease, Juvenile Gaucher

Disease, Neuronopathic Gaucher

Disease, Non-Neuronopathic Gaucher

Diseases, Gauchers

Diseases, Glucocerebrosidase Deficiency

GBA Deficiencies

GBA Deficiency

Gaucher Disease Type 1

Gaucher Disease Type 2

Gaucher Disease Type 3

Gaucher Disease, Acute Neuronopathic

Gaucher Disease, Acute Neuronopathic Type

Gaucher Disease, Chronic

Gaucher Disease, Chronic Neuronopathic Type

Gaucher Disease, Infantile

Gaucher Disease, Infantile Cerebral

Gaucher Disease, Juvenile

Gaucher Disease, Juvenile and Adult, Cerebral

Gaucher Disease, Neuronopathic

Gaucher Disease, Non Neuronopathic Form

Gaucher Disease, Non-Neuronopathic

Gaucher Disease, Non-Neuronopathic Form

Gaucher Disease, Noncerebral Juvenile

Gaucher Disease, Subacute Neuronopathic Form

Gaucher Disease, Subacute Neuronopathic Type

Gaucher Disease, Type 1

Gaucher Disease, Type 2

Gaucher Disease, Type 3

Gaucher Disease, Type I

Gaucher Disease, Type II

Gaucher Disease, Type III

Gaucher Splenomegaly

Gaucher Syndrome

Gaucher's Disease

Gauchers Disease

Gauchers Diseases

Glucocerebrosidase Deficiencies

Glucocerebrosidase Deficiency

Glucocerebrosidase Deficiency Disease

Glucocerebrosidase Deficiency Diseases



Glucosyl Cerebroside Lipidoses

Glucosyl Cerebroside Lipidosis

Glucosylceramidase Deficiency

Glucosylceramide Beta-Glucosidase Deficiency

Glucosylceramide Beta-Glucosidase Deficiency Disease

Glucosylceramide Lipidoses

Glucosylceramide Lipidosis

Histiocytoses, Kerasin

Histiocytoses, Lipoid (Kerasin Type)

Histiocytosis, Kerasin

Histiocytosis, Lipoid (Kerasin Type)

Infantile Gaucher Disease

Juvenile Gaucher Disease

Kerasin Histiocytoses

Kerasin Histiocytosis

Kerasin Lipoidoses

Kerasin Lipoidosis

Kerasin thesaurismoses

Kerasin thesaurismosis

Lipidoses, Glucosyl Cerebroside

Lipidoses, Glucosylceramide

Lipidosis Syndrome, Cerebroside

Lipidosis Syndromes, Cerebroside

Lipidosis, Glucosyl Cerebroside

Lipidosis, Glucosylceramide

Lipoid Histiocytoses (Kerasin Type)

Lipoid Histiocytosis (Kerasin Type)

Lipoidoses, Kerasin

Lipoidosis, Kerasin

Neuronopathic Gaucher Disease

Non Neuronopathic Gaucher Disease

Non-Neuronopathic Gaucher Disease

Splenomegaly, Gaucher

Subacute Neuronopathic Gaucher Disease

Syndrome, Cerebroside Lipidosis

Syndrome, Gaucher

Syndromes, Cerebroside Lipidosis

Type 1 Gaucher Disease

Type 2 Gaucher Disease

Type 3 Gaucher Disease

thesaurismoses, Kerasin

thesaurismosis, Kerasin

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.