Where can I read more about the diseases and traits covered in my direct-to-consumer genetic testing report |
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التاريخ: 30-10-2020
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Where can I read more about the diseases and traits covered in my direct-to-consumer genetic testing report ?
Learn more from Genetics Home Reference about the health conditions and traits included in your report. Each plain-language summary provides information about the condition’s major features, frequency, causes, and inheritance. You will also find links to other reputable sources of online health information.
Health conditions
BRCA1- or BRCA2-related breast cancer and ovarian cancer
Age-related macular degeneration
Alpha-1 antitrypsin deficiency
Celiac disease
Glucose-6-phosphate dehydrogenase deficiency, also called G6PD deficiency
Hereditary hemochromatosis
Hereditary thrombophilia: prothrombin thrombophilia and factor V Leiden
thrombophilia
Alzheimer disease
Parkinson disease
Wellness
Lactose intolerance
Traits
Cheek dimples
Eye color
Hair texture
Hair color (light or dark hair)
Carrier status
Autosomal recessive spastic ataxia of Charlevoix-Saguenay, also called
ARSACS
Andermann syndrome, also called agenesis of the corpus callosum with
peripheral neuropathy
Polycystic kidney disease
Beta thalassemia
Bloom syndrome
Canavan disease
PMM2-congenital disorder of glycosylation, also called PMM2-CDG
Cystic fibrosis
D-bifunctional protein deficiency
Dihydrolipoamide dehydrogenase deficiency
Familial dysautonomia
Congenital hyperinsulinism, also called familial hyperinsulinism
Fanconi anemia
GRACILE syndrome
Gaucher disease
Glycogen storage disease type I
Hereditary fructose intolerance
Junctional epidermolysis bullosa
Leigh syndrome
Limb-girdle muscular dystrophy
Medium-chain acyl-CoA dehydrogenase deficiency, also called MCAD deficiency
Maple syrup urine disease
Mucolipidosis type IV
CLN5 disease, also called neuronal ceroid lipofuscinosis (CLN5-related)
CLN1 disease, also called neuronal ceroid lipofuscinosis (PPT1-related)
Niemann-Pick disease
Nijmegen breakage syndrome
Nonsyndromic hearing loss
Pendred syndrome
Phenylketonuria
Primary hyperoxaluria
Rhizomelic chondrodysplasia punctata
Sialic acid storage disease, including Salla disease
Sickle cell disease, also called sickle cell anemia
Sjögren-Larsson syndrome
Tay-Sachs disease
Tyrosinemia
Usher syndrome
Zellweger spectrum disorder, also called Zellweger syndrome spectrum
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