Terminology Service < Semantic Lookup Platform

All terms in CLO

Label	Id	Description
RCB3052 cell	CLO_0051001	[Register: Fukuda, Hiroshi, Derived from tissue: blood in animal: human.]
GM11385 cell	CLO_0026088	[ CHROMOSOME DELETION PRADER-WILLI SYNDROME; PWS]
RCB0496 cell	CLO_0051000	[Originator: Kishi, Kenji, Register: Mizusawa, Hiroshi, Derived from tissue: blood in animal: human.]
GM11383 cell	CLO_0026087	[ PRADER-WILLI SYNDROME; PWS]
GM11387 cell	CLO_0026086	[ PRADER-WILLI SYNDROME; PWS]
carbonate	CHEBI_41609
carbon oxoanion	CHEBI_35604
hydrogencarbonate	CHEBI_17544
GM11386 cell	CLO_0026085	[ PRADER-WILLI SYNDROME; PWS]
heterocyclic compound	CHEBI_5686
Saimiri sciureus sciureus	NCBITaxon_190117
Saimiri sciureus	NCBITaxon_9521
Ewings sarcoma	EFO_0000174	[A spectrum of malignant tumors, affecting mostly males under age 20, characterized morphologically by the presence of small round cells. Ewing sarcoma and peripheral primitive neuroectodermal tumor represent the ends of a spectrum, with Ewing sarcoma lacking evidence of neural differentiation and the markers that characterize the peripheral primitive neuroectodermal tumor. Ewing sarcoma and peripheral primitive neuroectodermal tumor may share cytogenetic abnormalities, proto-oncogene expression, cell culture and immunohistochemical abnormalities. These tumors may occur in the soft tissues or the bones. Pain and the presence of a mass are the most common clinical symptoms. -- 2004 , A small round cell tumor that lacks morphologic, immunohistochemical, and electron microscopic evidence of neuroectodermal differentiation. It represents one of the two ends of the spectrum called Ewing's sarcoma/peripheral neuroectodermal tumor. It affects mostly males under age 20, and it can occur in soft tissue or bone. Pain and the presence of a mass are the most common clinical symptoms., A spectrum of malignant tumors, affecting mostly males under age 20, characterized morphologically by the presence of small round cells. Ewing sarcoma and peripheral primitive neuroectodermal tumor represent the ends of a spectrum, with Ewing sarcoma lacking evidence of neural differentiation and the markers that characterize the peripheral primitive neuroectodermal tumor. Ewing sarcoma and peripheral primitive neuroectodermal tumor may share cytogenetic abnormalities, proto-oncogene expression, cell culture and immunohistochemical abnormalities. These tumors may occur in the soft tissues or the bones. Pain and the presence of a mass are the most common clinical symptoms., A malignant tumor of the bone which always arises in the medullary tissue, occurring more often in cylindrical bones. There are conspicuous foci of necrosis in association with irregular masses of small, regular, rounded or ovoid cells with very scanty cytoplasm. The tumor occurs usually before the age of 20, about twice as frequently in males as in females. (From Dorland, 27th ed; Stedman, 25th ed)]
neuroectodermal tumor	DOID_171
GM11397 cell	CLO_0026095	[ TRANSLOCATED CHROMOSOME]
DA03015 cell	CLO_0014095	[ DIABETES MELLITUS FAMILY SAMPLE]
GM11405 cell	CLO_0026094	[ ANGELMAN SYNDROME; AS]
GM21583 cell	CLO_0014096	[ INTERNATIONAL HAPMAP PROJECT - MAASAI IN KINYAWA, KENYA INTERNATIONAL HAPMAP PROJECT - MAASAI IN KINYAWA, KENYA (PLATE I)]
GM11404 cell	CLO_0026093	[ ANGELMAN SYNDROME; AS CHROMOSOME DELETION]
Angelman syndrome	DOID_1932