KB_Bio_101

Last uploaded: January 21, 2014

Id	http://www.projecthalo.com/aura#Cystic-Fibrosis http://www.projecthalo.com/aura#Cystic-Fibrosis
Preferred Name	Cystic-Fibrosis
Type	http://www.w3.org/2002/07/owl#Class

user-description	A human genetic disorder caused by a recessive allele for a chloride channel protein; characterized by an excessive secretion of mucus and consequent vulnerability to infection; fatal if untreated.
prefLabel	Cystic-Fibrosis
prefixIRI	Cystic-Fibrosis
subClassOf	http://www.projecthalo.com/aura#Human-Genetic-Disorder
type	http://www.w3.org/2002/07/owl#Class
disjointWith	http://www.projecthalo.com/aura#Sex-Linked-Human-Genetic-Disorder http://www.projecthalo.com/aura#Tay-Sachs-disease http://www.projecthalo.com/aura#Sickle-Cell-Anemia http://www.projecthalo.com/aura#Phenylketonuria http://www.projecthalo.com/aura#Turner-Syndrome http://www.projecthalo.com/aura#Prader-Willi-Syndrome http://www.projecthalo.com/aura#Klinefelter-Syndrome http://www.projecthalo.com/aura#Down-Syndrome http://www.projecthalo.com/aura#Polydactyly http://www.projecthalo.com/aura#Triple-X http://www.projecthalo.com/aura#Huntingtons-Disease http://www.projecthalo.com/aura#Multifactorial-Genetic-Disorder See more See less

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