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	Gaucher Disease, Acute Neuronopathic Type -- See 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		1
	Gaucher Disease, Chronic -- See 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		1
	Gaucher Disease, Chronic Neuronopathic Type -- See 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		1
	Gaucher disease -- Diagnosis : Advances in Gaucher disease : basic and clinical perspectives / editor, Gregory A. Grabowski	2013	1
	Gaucher Disease, Infantile -- See 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		1
	Gaucher Disease, Infantile Cerebral -- See 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		1
	Gaucher Disease, Juvenile -- See 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		1
	Gaucher Disease, Juvenile and Adult, Cerebral -- See 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		1
	Gaucher Disease, Neuronopathic -- See 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		1
	Gaucher Disease, Non-Neuronopathic -- See 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		1
	Gaucher Disease, Non Neuronopathic Form -- See 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		1
	Gaucher Disease, Noncerebral Juvenile -- See 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		1
	Gaucher Disease, Subacute Neuronopathic Form -- See 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		1
	Gaucher Disease, Subacute Neuronopathic Type -- See 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		1
	Gaucher Disease -- therapy : Advances in Gaucher disease : basic and clinical perspectives / editor, Gregory A. Grabowski	2013	1
	Gaucher disease -- Treatment : Advances in Gaucher disease : basic and clinical perspectives / editor, Gregory A. Grabowski	2013	1
	Gaucher Disease, Type 1 -- See 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		1
	Gaucher Disease, Type 2 -- See 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		1
	Gaucher Disease Type 3 -- See 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		1
	Gaucher Disease, Type I -- See 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		1
	Gaucher Disease, Type II -- See 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		1
	Gaucher Disease, Type III -- See 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		1
	Gaucher-Schlagenhaufer syndrome -- See Gaucher disease		1
	Gaucher Splenomegaly -- See 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		1
	Gaucher Syndrome -- See 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		1
	Gaucher's disease -- 2 Related Subjects		2
	Gauchers Diseases -- See 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		1
	Gauchet, Marcel		2
	Gauchet, Marcel -- Political and social views : The Anthropological Turn French Political Thought After 1968	2020	1
	Gauchos -- See Also Cowboys		1
	Gauchos		7
	Gauchos -- Argentina -- Clara -- History : The invention of the Jewish gaucho : Villa Clara and the construction of Argentine identity / Judith Noemí Freidenberg ; foreword by June Nash	2009	1
	Gauchos -- Argentina -- History		2
	Gauchos -- Argentina -- La Rioja (Province) -- History -- 19th century : Children of Facundo : caudillo and gaucho insurgency during the Argentine state-formation process (La Rioja, 1853-1870) / Ariel de la Fuente	2000	1
	Gauchos -- Drama. : The Gaucho / the Elton Corporation ; United Artists ; director, F. Richard Jones ; written by Lotta Woods, based on a story by Elton Thomas	2001	1
	Gauchos in literature.		3
	Gerchunoff, Alberto, 1883-1950. Gauchos judíos : Parricide on the Pampa? A New Study and Translation of Alberto Gerchunoff's Los Gauchos Judíos	2015	1
	Gauchos -- Poetry : The gaucho Martín Fierro / English translation, by Frank G. Carrino, Alberto J. Carlos [and] Norman Mangouni	1974	1
	Gaud[i, Antoni, 1852-1926 -- Themes, motives : Antoni Gaudi / [authors: Aurora Cuito, Cristina Montes ; translation: Juliet King, Bettina Beck]	2002	1
	Gauḍa -- See Gauḍapāda Ācārya		1
	Gauḍapāda Ācārya, active 7th century -- See Gauḍapāda Ācārya		1
	Āgamaśāstra -- See Gauḍapādakārikā		1
	Āgamaśāstram -- See Gauḍapādakārikā		1
	Gauḍapāda Ācārya. Gauḍapādakārikā.		2
	Gauḍapādīyam Āgamaśāstram -- See Gauḍapādakārikā		1
	Gauḍapāda Ācārya -- Knowledge -- Mahayana Buddhism : Early Advaita Vedānta and Buddhism : the Mahāyāna context of the Gauḍapādīya-kārikā / Richard King	1995	1
	Māṇḍūkyagauḍapādīyam -- See Gauḍapādakārikā		1
	Māṇḍūkyakārikā -- See Gauḍapādakārikā		1
	Māṇḍūkyopaniṣatkārikā -- See Gauḍapādakārikā		1
	Gauḍapāda Ācārya -- Sources. : Early Advaita Vedānta and Buddhism : the Mahāyāna context of the Gauḍapādīya-kārikā / Richard King	1995	1
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Gaucher Disease, Acute Neuronopathic Type -- See Gaucher Disease

Gaucher Disease, Chronic -- See Gaucher Disease

Gaucher Disease, Chronic Neuronopathic Type -- See Gaucher Disease

Gaucher Disease, Infantile -- See Gaucher Disease

Gaucher Disease, Infantile Cerebral -- See Gaucher Disease

Gaucher Disease, Juvenile -- See Gaucher Disease

Gaucher Disease, Juvenile and Adult, Cerebral -- See Gaucher Disease

Gaucher Disease, Neuronopathic -- See Gaucher Disease

Gaucher Disease, Non-Neuronopathic -- See Gaucher Disease

Gaucher Disease, Non Neuronopathic Form -- See Gaucher Disease

Gaucher Disease, Noncerebral Juvenile -- See Gaucher Disease

Gaucher Disease, Subacute Neuronopathic Form -- See Gaucher Disease

Gaucher Disease, Subacute Neuronopathic Type -- See Gaucher Disease

Gaucher Disease, Type 1 -- See Gaucher Disease

Gaucher Disease, Type 2 -- See Gaucher Disease

Gaucher Disease Type 3 -- See Gaucher Disease

Gaucher Disease, Type I -- See Gaucher Disease

Gaucher Disease, Type II -- See Gaucher Disease

Gaucher Disease, Type III -- See Gaucher Disease

Gaucher-Schlagenhaufer syndrome -- See Gaucher disease

Gaucher Splenomegaly -- See Gaucher Disease

Gaucher Syndrome -- See Gaucher Disease

Gauchers Diseases -- See Gaucher Disease

Gauchos -- See Also Cowboys

Gauḍa -- See Gauḍapāda Ācārya

Gauḍapāda Ācārya, active 7th century -- See Gauḍapāda Ācārya

Āgamaśāstra -- See Gauḍapādakārikā

Āgamaśāstram -- See Gauḍapādakārikā

Gauḍapādīyam Āgamaśāstram -- See Gauḍapādakārikā

Māṇḍūkyagauḍapādīyam -- See Gauḍapādakārikā

Māṇḍūkyakārikā -- See Gauḍapādakārikā

Māṇḍūkyopaniṣatkārikā -- See Gauḍapādakārikā