Category:Genetic disorders
Subcategories
This category has the following 10 subcategories, out of 10 total.
Pages in category "Genetic disorders"
The following 200 pages are in this category, out of 1,744 total.
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- Adrenal atrophy CT
- Adrenal atrophy differential diagnosis
- Adrenal atrophy electrocardiogram
- Adrenal atrophy epidemiology and demographics
- Adrenal atrophy future or investigational therapies
- Adrenal atrophy historical perspective
- Adrenal atrophy laboratory findings
- Adrenal atrophy medical therapy
- Adrenal atrophy MRI
- Adrenal atrophy natural history, complications and prognosis
- Adrenal atrophy other diagnostic studies
- Adrenal atrophy other imaging findings
- Adrenal atrophy overview
- Adrenal atrophy physical examination
- Adrenal atrophy primary prevention
- Adrenal atrophy risk factors
- Adrenal atrophy screening
- Adrenal atrophy secondary prevention
- Adrenal atrophy surgery
- Adrenal atrophy ultrasound
- Adrenal atrophy x ray
- Adrenoleukodystrophy (patient information)
- Adult treatment panel guidelines (ATP III) for hypercholestrolemia
- African iron overload
- ALA dehydratase deficiency
- Alagille syndrome
- Alagille syndrome associated conditions
- Alagille syndrome laboratory tests
- Alagille syndrome overview
- Alkaptonuria
- Alkaptonuria (patient information)
- Allan-Herndon-Dudley syndrome
- Alpha 1-antitrypsin deficiency (patient information)
- Alport syndrome
- Alport syndrome case study one
- Alport syndrome causes
- Alport syndrome cost-effectiveness of therapy
- Alport syndrome diagnostic criteria
- Alport syndrome differential diagnosis
- Alport syndrome echocardiography or ultrasound
- Alport syndrome epidemiology and demographics
- Alport syndrome future or investigational therapies
- Alport syndrome historical perspective
- Alport syndrome history and symptoms
- Alport syndrome laboratory findings
- Alport syndrome medical therapy
- Alport syndrome natural history, complications and prognosis
- Alport syndrome other diagnostic studies
- Alport syndrome overview
- Alport syndrome pathophysiology
- Alport syndrome physical examination
- Alport syndrome primary prevention
- Alport syndrome secondary prevention
- Alport syndrome surgery
- Amblyopia (patient information)
- Amelogenesis imperfecta
- Amyotrophic lateral sclerosis (patient information)
- Anaplastic thyroid cancer biopsy
- Anaplastic thyroid cancer causes
- Anaplastic thyroid cancer chest x ray
- Anaplastic thyroid cancer CT
- Anaplastic thyroid cancer differential diagnosis
- Anaplastic thyroid cancer echocardiography or ultrasound
- Anaplastic thyroid cancer epidemiology and demographics
- Anaplastic thyroid cancer historical perspective
- Anaplastic thyroid cancer history and symptoms
- Anaplastic thyroid cancer laboratory findings
- Anaplastic thyroid cancer medical therapy
- Anaplastic thyroid cancer MRI
- Anaplastic thyroid cancer natural history, complications and prognosis
- Anaplastic thyroid cancer other diagnostic studies
- Anaplastic thyroid cancer other imaging findings
- Anaplastic thyroid cancer overview
- Anaplastic thyroid cancer pathophysiology
- Anaplastic thyroid cancer physical examination
- Anaplastic thyroid cancer prevention
- Anaplastic thyroid cancer risk factors
- Anaplastic thyroid cancer staging
- Anaplastic thyroid cancer surgery
- Andersen-Tawil syndrome
- Andersen-Tawil syndrome classification
- Andersen-Tawil syndrome diagnostic criteria
- Andersen-Tawil syndrome differential diagnosis
- Andersen-Tawil syndrome electrocardiogram
- Andersen-Tawil syndrome historical perspective
- Andersen-Tawil syndrome history and symptoms
- Andersen-Tawil syndrome laboratory findings
- Andersen-Tawil syndrome medical therapy
- Andersen-Tawil syndrome other diagnostic studies
- Andersen-Tawil syndrome other imaging findings
- Andersen-Tawil syndrome overview
- Andersen-Tawil syndrome pathophysiology
- Andersen-Tawil syndrome physical examination
- Andersen-Tawil syndrome primary prevention
- Andersen-Tawil syndrome secondary prevention
- Andersen-Tawil syndrome tertiary prevention
- Androgen insensitivity syndrome case study one
- Androgenic alopecia
- Aneuploidy
- Antenatal detection and diagnosis
- Anticipation (genetics)
- Antley-Bixler syndrome
- Apert syndrome
- Apparent mineralocorticoid excess
- Arakawa's syndrome II
- Arginemia
- Asperger syndrome
- Asperger syndrome behavioral therapy
- Asperger syndrome case study one
- Asperger syndrome causes
- Asperger syndrome classification
- Asperger syndrome cost-effectiveness of therapy
- Asperger syndrome differential diagnosis
- Asperger syndrome epidemiology and demographics
- Asperger syndrome future or investigational therapies
- Asperger syndrome historical perspective
- Asperger syndrome history and symptoms
- Asperger syndrome laboratory findings
- Asperger syndrome medical therapy
- Asperger syndrome natural history, complications and prognosis
- Asperger syndrome other diagnostic studies
- Asperger syndrome overview
- Asperger syndrome pathophysiology
- Asperger syndrome physical examination
- Asperger syndrome risk factors
- Asperger syndrome screening
- Asymptomatic carrier
- Ataxia (patient information)
- Ataxia telangiectasia
- Ataxia telangiectasia (patient information)
- Ataxia telangiectasia case study one
- Ataxia telangiectasia causes
- Ataxia telangiectasia classification
- Ataxia telangiectasia cost-effectiveness of therapy
- Ataxia telangiectasia CT
- Ataxia telangiectasia differential diagnosis
- Ataxia telangiectasia epidemiology and demographics
- Ataxia telangiectasia future or investigational therapies
- Ataxia telangiectasia historical perspective
- Ataxia telangiectasia history and symptoms
- Ataxia telangiectasia laboratory findings
- Ataxia telangiectasia medical therapy
- Ataxia telangiectasia MRI
- Ataxia telangiectasia natural history, complications and prognosis
- Ataxia telangiectasia other diagnostic studies
- Ataxia telangiectasia overview
- Ataxia telangiectasia pathophysiology
- Ataxia telangiectasia physical examination
- Ataxia telangiectasia risk factors
- Ataxia telangiectasia screening
- Atelosteogenesis, type II
- Atransferrinemia
- Autosomal dominant nocturnal frontal lobe epilepsy
B
- Barakat syndrome
- Bardet-Biedl syndrome
- Bare lymphocyte syndrome 2
- Barraquer-Simons syndrome
- Bartter syndrome
- Bartter syndrome (patient information)
- Bartter syndrome case study one
- Bartter syndrome causes
- Bartter syndrome cost-effectiveness of therapy
- Bartter syndrome CT
- Bartter syndrome differential diagnosis
- Bartter syndrome echocardiography or ultrasound
- Bartter syndrome electrocardiogram
- Bartter syndrome epidemiology and demographics
- Bartter syndrome future or investigational therapies
- Bartter syndrome historical perspective
- Bartter syndrome history and symptoms
- Bartter syndrome laboratory findings
- Bartter syndrome medical therapy
- Bartter syndrome MRI
- Bartter syndrome natural history, complications and prognosis
- Bartter syndrome other diagnostic studies
- Bartter syndrome other imaging findings
- Bartter syndrome overview
- Bartter syndrome pathophysiology
- Bartter syndrome physical examination
- Bartter syndrome risk factors
- Bartter syndrome surgery
- Bartter syndrome x ray
- Beals syndrome
- Becker's muscular dystrophy
- Beckwith-Wiedemann syndrome
- Beckwith-Wiedemann syndrome (patient information)
- Behr's syndrome
- Benign familial neonatal convulsions
- Beta-ketothiolase deficiency
- Beta-mannosidosis
- Beta-thalassemia
- Beta-thalassemia (patient information)
- Beta-thalassemia case study one
- Beta-thalassemia classification
- Beta-thalassemia cost-effectiveness of therapy
- Beta-thalassemia CT
- Beta-thalassemia differential diagnosis
- Beta-thalassemia epidemiology and demographics
- Beta-thalassemia future or investigational therapies
- Beta-thalassemia historical perspective