Category:Genetic Disease
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Please classify all genetic diseases and syndromes appropriately by including the text [[Category:Genetic Disease]] somewhere on the page.
Pages in category "Genetic Disease"
The following 200 pages are in this category, out of 208 total.
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- ACC/AHA guidelines-recommendations for permanent pacing in patients with congenital heart disease
- Achondrogenesis
- Acrodermatitis enterohepatica
- Adelaide-Type Craniosynostosis
- ALA Dehydratase Deficiency
- Alkaptonuria
- Alstrom syndrome
- Alstrom syndrome (patient information)
- Alstrom syndrome case study one
- Alstrom syndrome chest x ray
- Alstrom syndrome cost-effectiveness of therapy
- Alstrom syndrome CT
- Alstrom syndrome diagnostic criteria
- Alstrom syndrome differential diagnosis
- Alstrom syndrome echocardiography or ultrasound
- Alstrom syndrome electrocardiogram
- Alstrom syndrome epidemiology and demographics
- Alstrom syndrome future or investigational therapies
- Alstrom syndrome historical perspective
- Alstrom syndrome history and symptoms
- Alstrom syndrome laboratory findings
- Alstrom syndrome medical therapy
- Alstrom syndrome MRI
- Alstrom syndrome natural history, complications and prognosis
- Alstrom syndrome other diagnostic studies
- Alstrom syndrome other imaging findings
- Alstrom syndrome overview
- Alstrom syndrome pathophysiology
- Alstrom syndrome physical examination
- Alstrom syndrome primary prevention
- Alstrom syndrome screening
- Alstrom syndrome surgery
- Alstrom syndrome tertiary prevention
- Amelogenesis Imperfecta
- Amelogenesis imperfecta
- Androgen insensitivity syndrome case study one
- Arachnodactyly
- Autosomal recessive
C
- CADASIL
- Cardiomyopathy
- Cardiomyopathy (patient information)
- Cardiomyopathy causes
- Cardiomyopathy chest x ray
- Cardiomyopathy classification
- Cardiomyopathy CT
- Cardiomyopathy differential diagnosis
- Cardiomyopathy echocardiography or ultrasound
- Cardiomyopathy electrocardiogram
- Cardiomyopathy epidemiology and demographics
- Cardiomyopathy historical perspective
- Cardiomyopathy history and symptoms
- Cardiomyopathy laboratory findings
- Cardiomyopathy medical therapy
- Cardiomyopathy MRI
- Cardiomyopathy natural history, complications and prognosis
- Cardiomyopathy other diagnostic studies
- Cardiomyopathy other imaging findings
- Cardiomyopathy overview
- Cardiomyopathy pathophysiology
- Cardiomyopathy physical examination
- Cardiomyopathy primary prevention
- Cardiomyopathy risk factors
- Cardiomyopathy secondary prevention
- Cardiomyopathy surgery
- Charcot-Marie-Tooth disease
- Charcot-Marie-Tooth Syndrome
- Chromosome
- Collagenopathy, types II and XI
- Congenital Absence of the Vas Deferens
- Congenital absence of the vas deferens
- Congenital anorchia
- Congenital heart disease ACC/AHA guidelines
- Congenital heart disease ACC/AHA guidelines for management of adults
- Congenital heart disease ACC/AHA guidelines for permanent pacing
- Congenital heart disease cyanotic
- Connective tissue disease
- Crouzonodermoskeletal syndrome
- Cyanotic heart defect case study one
- Cyanotic heart defect causes
- Cyanotic heart defect chest x ray
- Cyanotic heart defect cost-effectiveness of therapy
- Cyanotic heart defect CT
- Cyanotic heart defect differential diagnosis
- Cyanotic heart defect echocardiography or ultrasound
- Cyanotic heart defect electrocardiogram
- Cyanotic heart defect epidemiology and demographics
- Cyanotic heart defect future or investigational therapies
- Cyanotic heart defect historical perspective
- Cyanotic heart defect medical therapy
- Cyanotic heart defect MRI
- Cyanotic heart defect natural history, complications and prognosis
- Cyanotic heart defect other diagnostic studies
- Cyanotic heart defect other imaging findings
- Cyanotic heart defect pathophysiology
- Cyanotic heart defect physical examination
- Cyanotic heart defect primary prevention
- Cyanotic heart defect risk factors
- Cyanotic heart defect screening
F
- Fabry's disease
- Fabry's disease MRI
- Familial adenomatous polyposis case study one
- Familial adenomatous polyposis chest x ray
- Familial adenomatous polyposis cost-effectiveness of therapy
- Familial adenomatous polyposis CT
- Familial adenomatous polyposis future or investigational therapies
- Familial adenomatous polyposis ultrasound
M
P
- Point mutation
- Postnatal Detection and Diagnosis
- Protein C deficiency case study one
- Pseudoxanthoma elasticum
- Pseudoxanthoma elasticum (patient information)
- Pseudoxanthoma elasticum causes
- Pseudoxanthoma elasticum classification
- Pseudoxanthoma elasticum differential diagnosis
- Pseudoxanthoma elasticum epidemiology and demographics
- Pseudoxanthoma elasticum future or investigational therapies
- Pseudoxanthoma elasticum historical perspective
- Pseudoxanthoma elasticum history and symptoms
- Pseudoxanthoma elasticum laboratory findings
- Pseudoxanthoma elasticum medical therapy
- Pseudoxanthoma elasticum natural history, complications and prognosis
- Pseudoxanthoma elasticum other imaging findings
- Pseudoxanthoma elasticum overview
- Pseudoxanthoma elasticum pathophysiology
- Pseudoxanthoma elasticum physical examination
- Pseudoxanthoma elasticum primary prevention
- Pseudoxanthoma elasticum surgery
S
- SADDAN
- Single transverse palmar crease
- Spondyloepimetaphyseal dysplasia, Strudwick type
- Swyer's syndrome
- Swyer's syndrome case study one
- Swyer's syndrome causes
- Swyer's syndrome classification
- Swyer's syndrome cost-effectiveness of therapy
- Swyer's syndrome CT
- Swyer's syndrome differential diagnosis
- Swyer's syndrome echocardiography or ultrasound
- Swyer's syndrome epidemiology and demographics
- Swyer's syndrome future or investigational therapies
- Swyer's syndrome historical perspective
- Swyer's syndrome history and symptoms
- Swyer's syndrome laboratory findings
- Swyer's syndrome medical therapy
- Swyer's syndrome MRI
- Swyer's syndrome natural history, complications and prognosis
- Swyer's syndrome other diagnostic studies
- Swyer's syndrome other imaging findings
- Swyer's syndrome overview
- Swyer's syndrome pathophysiology
- Swyer's syndrome physical examination
- Swyer's syndrome prevention
- Swyer's syndrome risk factors
- Swyer's syndrome surgery
- Swyer's syndrome x ray
T
- Tetrahydrobiopterin deficiency
- Tetralogy of fallot electrocardiogram
- Thanatophoric dysplasia
- Transposition of the great arteries differential diagnosis
- Transposition of the great vessels epidemiology and demographics
- Transposition of the great vessels historical perspective
- Transposition of the great vessels overview
- Transposition of the great vessels risk factors
- Transposition of the great vessels screening
V
- Variegate porphyria
- Ventricular septal defect
- Ventricular septal defect Diagram of ventricular septal defect
- Ventricular septal defect image 1-interventricular septal defect (muscular septum)
- Ventricular septal defect image 2-subvalvular ventricular septal defect
- Ventricular septal defect image 3- gross, infant heart, pulmonary outlet, muscular septal defect