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Metadata
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About:
Genetics
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An Entity of Type :
owl:Thing
, within Data Space :
134.155.108.49:8890
associated with source
dataset(s)
Attributes
Values
rdfs:label
Genetics
is
dcterms:subject
of
Familial Mediterranean fever
Sialidosis
Ebstein's anomaly
Ataxia telangiectasia
Fucosidosis
Cytogenetics
Gaucher's disease
Selective immunoglobulin A deficiency
Osteopetrosis
Tourette Syndrome
Porphyria
Psoriasis
Gene
De Vivo disease
Congenital adrenal hyperplasia
Noonan syndrome
Patau syndrome
Williams syndrome
Phenylketonuria
Albinism
Transheterozygote
Glycogen storage disease type V
RNA
Allele
Alexander disease
Leukoencepalopathy
Hereditary hemorrhagic telangiectasia
Familial hypercholesterolemia
Color blindness
Polycystic kidney disease
Fabry disease
Genetic recombination
Mitotic crossover
Li-Fraumeni syndrome
Spinal muscular atrophy
Trisomy-21
X-inactivation
Centromere
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Adrenoleukodystrophy
Brugada syndrome
Familial dysautonomia
Von Willebrand disease
Gaucher’s disease
Caroli disease
Blind uterus
Drosophila melanogaster
Lesch-Nyhan syndrome
Neuronal ceroid lipofuscinosis
Mutagen
Trisomy
MELAS syndrome
Turner Syndrome
Von Hippel-Lindau Syndrome
MERRF syndrome
Lafora disease
Persistent Mullerian duct syndrome
Kallmann syndrome
Marfan syndrome
McLeod syndrome
Heterochromia
Hemophilia
DiGeorge syndrome
Factor V Leiden
Familial adenomatous polyposis
Transgene
Genotype
Hereditary nonpolyposis colorectal cancer
Hypertrichosis
DNA
Sickle Cell Anemia
Mutation
CIPA
Fatal familial insomnia
Unverricht-Lundborg disease
Cancer syndrome
Gerstmann-Sträussler-Scheinker syndrome
Wilson's disease
FLP-FRT recombination
Muckle-Wells syndrome
Krabbe disease
Hereditary sensory autonomic neuropathy type 1
Hemochromatosis
Nondisjunction
Tuberous sclerosis
Alpha 1-antitrypsin deficiency
Metachromatic leukodystrophy
Osteogenesis imperfecta
Chromosome
Klinefelter syndrome
Genetic mosaicism
Hyperimmunoglobulin E syndrome
Neurofibromatosis
Bernard-Soulier syndrome
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