About: Chromosome 18 Short Arm

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About: Chromosome 18 Short Arm Goto Sponge NotDistinct Permalink

An Entity of Type : about:nusq#this, within Data Space : semmed.demo.openlinksw.com associated with source document(s)

Attributes	Values
type	nusq
label	Chromosome 18 Short Arm chromosome 18 short arm
http://semmed.demo...com/terms#part_of	Individual
http://semmed.demo...s#associated_with	Carcinoma, Transitional Cell Dystonia
http://semmed.demo...terms#location_of	Trisomy
terms:part_of	C0030705 Upper Extremity Human Cell Line Human Child Fetus Individual Mothers Girls Clone Cells Chromosomes sibling Satellite Viruses Ring Chromosomes Half-sister Chromosome 13 Short Arm
terms:causes	Edward's syndrome NOS DELETION
terms:location_of	Disease Diabetes Syndrome Schizophrenia Primary carcinoma of the liver cells Dystonia Musculorum Deformans Psychotic Disorders Somatotropin deficiency Psoriasis Bipolar Disorder Skin Diseases, Genetic Myopia Absence Epilepsy Chronic Childhood Arthritis Xeroderma Pigmentosum Febrile Convulsions Trisomy Severe myopia Dystonias, Sporadic Adenocarcinoma, endocervical type
terms:coexists_with	Macrophage Chemotactic Factors
terms:associated_with	Nondisjunction, Genetic Neoplasm Metastasis Edward's syndrome NOS adenoma Myeloid Leukemia, Chronic Colorectal Cancer DiGeorge Syndrome Carcinoma, Transitional Cell Loss of Heterozygosity Dystonia Mammary Neoplasms Dystonic Disorder Eye Manifestations Keratosis pilaris Moderate Mental Retardation Chordoid meningioma Deletion of short arm of chromosome 18 Keratosis pilaris atrophicans Adult-Onset Idiopathic Torsion Dystonias
terms:neg_associated_with	Symptoms Myopia Chordoid meningioma
terms:administered_to	Long-Term Survivors
LOCATION_OF	Somatotropin deficiency Bipolar Disorder Skin Diseases, Genetic Absence Epilepsy Xeroderma Pigmentosum Febrile Convulsions Dystonias, Sporadic
ASSOCIATED_WITH	adenoma Loss of Heterozygosity Dystonia Dystonic Disorder Eye Manifestations Keratosis pilaris Keratosis pilaris atrophicans
schema:identifier	C1520795 c1520795
PART_OF	C0030705 Individual Girls
is http://semmed.demo...terms#location_of of	Child Fetus Boys X Chromosome Chromosomes, Human, Pair 18
is http://semmed.demo...rms#coexists_with of	CFC1 gene\|CFC1
is terms:part_of of	Genes Tumor Suppressor Genes Quantitative Trait Loci TECR Phosphomannomutase
is terms:location_of of	Cells

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