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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- Beta-thalassemia history and symptoms
- Beta-thalassemia laboratory findings
- Beta-thalassemia medical therapy
- Beta-thalassemia MRI
- Beta-thalassemia natural history, complications and prognosis
- Beta-thalassemia other diagnostic studies
- Beta-thalassemia other imaging findings
- Beta-thalassemia overview
- Beta-thalassemia pathophysiology
- Beta-thalassemia physical examination
- Beta-thalassemia primary prevention
- Beta-thalassemia risk factors
- Beta-thalassemia secondary prevention
- Beta-thalassemia surgery
- Beta-thalassemia ultrasound
- Beta-thalassemia x ray
- Bietti's crystalline dystrophy
- Biotinidase deficiency
- Birt-Hogg-Dubé syndrome
- Bloom syndrome
- Blue diaper syndrome
- Boomerang dysplasia
- Branchio-oto-renal syndrome
- Brugada syndrome
- Brugada syndrome (patient information)
- Brugada syndrome case study one
- Brugada syndrome chest x ray
- Brugada syndrome classification
- Brugada syndrome cost-effectiveness of therapy
- Brugada syndrome diagnostic criteria
- Brugada syndrome differential diagnosis
- Brugada syndrome drugs to avoid
- Brugada syndrome drugs to preferably avoid
- Brugada syndrome echocardiography or ultrasound
- Brugada syndrome electrocardiogram
- Brugada syndrome electrocardiographic examples of Type I Brugada syndrome
- Brugada syndrome electrophysiologic studies
- Brugada syndrome epidemiology and demographics
- Brugada syndrome future or investigational therapies
- Brugada syndrome genetic testing
- Brugada syndrome historical perspective
- Brugada syndrome history and symptoms
- Brugada syndrome laboratory findings
- Brugada syndrome natural history, complications and prognosis
- Brugada syndrome overview
- Brugada syndrome pathophysiology
- Brugada syndrome physical examination
- Brugada syndrome risk factors
- Brugada syndrome screening
- Brugada syndrome treatment
C
- CADASIL
- CAMFAK syndrome
- Camptomelic dysplasia
- Camurati-Engelmann disease
- Carbamoyl phosphate synthetase I deficiency
- Cardiofaciocutaneous syndrome
- Carnitine-acylcarnitine translocase deficiency
- Carnosinemia
- Carpenter syndrome
- Cat eye syndrome
- Cavernous angioma
- Cavernous angioma case study one
- Cavernous angioma causes
- Cavernous angioma cost-effectiveness of therapy
- Cavernous angioma CT
- Cavernous angioma differential diagnosis
- Cavernous angioma epidemiology and demographics
- Cavernous angioma future or investigational therapies
- Cavernous angioma historical perspective
- Cavernous angioma history and symptoms
- Cavernous angioma MRA
- Cavernous angioma MRI
- Cavernous angioma natural history, complications and prognosis
- Cavernous angioma other diagnostic studies
- Cavernous angioma other imaging findings
- Cavernous angioma overview
- Cavernous angioma pathophysiology
- Cavernous angioma physical examination
- Cavernous angioma risk factors
- Cavernous angioma surgery
- Celiac disease
- Celiac disease (patient information)
- Celiac disease causes
- Celiac disease classification
- Celiac disease cost-effectiveness of therapy
- Celiac disease CT scan
- Celiac disease diagnostic criteria
- Celiac disease echocardiography and ultrasound
- Celiac disease electrocardiogram
- Celiac disease epidemiology and demographics
- Celiac disease future or investigational therapies
- Celiac disease historical perspective
- Celiac disease history and symptoms
- Celiac disease medical therapy
- Celiac disease MRI
- Celiac disease natural history, complications and prognosis
- Celiac disease other diagnostic studies
- Celiac disease other imaging findings
- Celiac disease overview
- Celiac disease pathophysiology
- Celiac disease physical examination
- Celiac disease risk factors
- Celiac disease screening
- Celiac disease x ray
- Central core disease
- Channelopathy
- Charcot-Marie-Tooth disease
- Cherubism
- Childhood absence epilepsy
- Chromosome 1, 1p36 deletion syndrome
- Chromosome 15q partial deletion
- Chromosome 15q trisomy
- Chromosome abnormality
- Chronic granulomatous disease
- Ciliopathy
- Cobb syndrome
- Cockayne syndrome
- Coffin-Siris syndrome
- Cohen syndrome
- Collagenopathy, types II and XI
- Color blindness
- Color blindness (patient information)
- Congenital adrenal hyperplasia causes
- Congenital adrenal hyperplasia chest x ray
- Congenital adrenal hyperplasia cost-effectiveness of therapy
- Congenital adrenal hyperplasia CT
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency case study one
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency cost-effectiveness of therapy
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency future or investigational therapies
- Congenital adrenal hyperplasia echocardiography or ultrasound
- Congenital adrenal hyperplasia electrocardiogram
- Congenital adrenal hyperplasia future or investigational therapies
- Congenital adrenal hyperplasia laboratory tests
- Congenital adrenal hyperplasia MRI
- Congenital adrenal hyperplasia natural history
- Congenital adrenal hyperplasia other diagnostic studies
- Congenital adrenal hyperplasia other imaging findings
- Congenital adrenal hyperplasia overview
- Congenital adrenal hyperplasia physical examination
- Congenital adrenal hyperplasia primary prevention
- Congenital adrenal hyperplasia risk factors
- Congenital adrenal hyperplasia secondary prevention
- Congenital disorder of glycosylation
- Congenital heart disease
- Congenital heart disease (patient information)
- Congenital heart disease case study one
- Congenital heart disease causes
- Congenital heart disease chest x ray
- Congenital heart disease classification
- Congenital heart disease congenital heart disease anatomy
- Congenital heart disease CT
- Congenital heart disease diagnosis
- Congenital heart disease differential diagnosis
- Congenital heart disease echocardiography
- Congenital heart disease electrocardiogram
- Congenital heart disease epidemiology and demographics
- Congenital heart disease history and symptoms
- Congenital heart disease laboratory findings
- Congenital heart disease medical therapy
- Congenital heart disease MRI
- Congenital heart disease natural history, complications and prognosis
- Congenital heart disease other imaging findings
- Congenital heart disease outcomes
- Congenital heart disease overview
- Congenital heart disease pathophysiology
- Congenital heart disease physical examination
- Congenital heart disease prenatal ultrasound
- Congenital heart disease prevention
- Congenital heart disease reproduction
- Congenital heart disease risk factors
- Congenital heart disease surgery
- Congenital hyperinsulinism
- Congenital hyperinsulinism (patient information)
- Congenital hyperinsulinism case study one
- Congenital hyperinsulinism causes
- Congenital hyperinsulinism classification
- Congenital hyperinsulinism cost-effectiveness of therapy
- Congenital hyperinsulinism CT
- Congenital hyperinsulinism differential diagnosis
- Congenital hyperinsulinism epidemiology and demographics
- Congenital hyperinsulinism future or investigational therapies
- Congenital hyperinsulinism historical perspective
- Congenital hyperinsulinism history and symptoms
- Congenital hyperinsulinism laboratory findings
- Congenital hyperinsulinism medical therapy
- Congenital hyperinsulinism MRI
- Congenital hyperinsulinism natural history, complications and prognosis
- Congenital hyperinsulinism other diagnostic studies
- Congenital hyperinsulinism other imaging findings
- Congenital hyperinsulinism overview
- Congenital hyperinsulinism pathophysiology
- Congenital hyperinsulinism physical examination
- Congenital hyperinsulinism primary prevention
- Congenital hyperinsulinism risk factors
- Congenital hyperinsulinism screening
- Congenital hyperinsulinism secondary prevention
- Congenital hyperinsulinism surgery
- Congenital hyperinsulinism ultrasound
- Congenital hyperinsulinism x ray
- Congenital hypothyroidism (patient information)