Category:Is a medical condition
From SNPedia
This page collects together medical conditions.
Pages in category "Is a medical condition"
The following 200 pages are in this category, out of 570 total.
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- Abdominal aortic aneurysm
- ABO blood group
- Acetylation
- Achondroplasia
- Acid reflux disease
- Acromegaly
- Acute intermittent porphyria
- Acute lymphoblastic leukemia
- Acute myeloid leukemia
- Addiction
- Addison's disease
- Age related macular degeneration
- Age-related hearing impairment
- Agenesis of the Corpus Callosum with Peripheral Neuropathy
- AIDS
- Alcoholism
- Alexander's disease
- Allergies
- Allograft rejection
- Alopecia Areata
- Alpha Thalassemia
- Alpha-1 antitrypsin deficiency
- Alpha-1-antitrypsin deficiency
- Alport syndrome
- Alzheimer's disease
- Amyloidosis
- Amyotrophic Lateral Sclerosis
- Amyotrophic lateral sclerosis 22 with or without frontotemporal dementia
- Andersen Tawil syndrome
- Androgen resistance syndrome
- Aneurysm
- Angioedema
- Ankylosing spondylitis
- Anorexia nervosa
- Antithrombin III deficiency
- Anxiety disorder
- Aphasia
- APOE2 VARIANT
- Argininosuccinate lyase deficiency
- Arrhythmogenic Right Ventricular Cardiomyopathy
- Arthritis
- Arylsulfatase A pseudodeficiency
- Asian flush
- Asperger syndrome
- Asthma
- Ataxia
- Atherosclerosis
- Atopic dermatitis
- Atorvastatin response - Efficacy
- Atrial fibrillation
- Attention deficit hyperactivity disorder
- Atypical hemolytic uremic syndrome
- Atypical hemolytic-uremic syndrome 1
- Autism
- Autoimmune disease
- Autoimmune hepatitis
- Autoimmune thyroid disease 3
- Autoimmune thyroiditis
- Autosomal dominant hypophosphatemic rickets
- Autosomal Recessive Polycystic Kidney Disease
- Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
B
- Baldness
- BAP1 tumor predisposition syndrome
- Bardet-Biedl syndrome
- Barth syndrome
- Bartter syndrome
- Basal cell carcinoma
- Basal ganglia calcification
- Batten disease
- Behçet's disease
- Benign familial neonatal-infantile seizures
- Beta Thalassemia
- Bicuspid aortic valve
- Bipolar disorder
- Birt-Hogg-Dube syndrome
- Bladder cancer
- Blau syndrome
- Blindness
- Blood
- Blood pressure
- Bloom syndrome
- Bowen-Conradi syndrome
- Breast cancer
- Breast-ovarian cancer
- Brown-Vialetto-Van laere syndrome
- Brugada syndrome
- Brugada syndrome 1
- Brugada syndrome 3
- Bupropion response - Efficacy
C
- Canavan disease
- Cancer
- Cancer progression and tumor cell motility
- Carbohydrate-deficient glycoprotein syndrome type II
- Cardiac arrhythmia
- Cardiac valvular dysplasia
- Carnitine palmitoyltransferase I deficiency
- Carpal tunnel syndrome
- Cataplexy and narcolepsy
- Cataracts
- CATECHOL-O-METHYLTRANSFERASE POLYMORPHISM
- Celiac disease
- Celiac disease 3
- Central core disease
- Cerebral amyloid angiopathy
- Cerebral cavernous malformation
- Cerebrovascular disease
- Cervical cancer
- Charcot-Marie-Tooth
- Charcot-Marie-Tooth disease
- Cholesterol
- Chondrodysplasia
- Chorionic plate inflammation
- Choroideremia
- Chronic fatigue syndrome
- Chronic kidney disease
- Chronic lower respiratory disease
- Chronic obstructive pulmonary disease
- Citrullinemia type I
- Cleft palate
- Cluster headaches
- Cockayne syndrome
- Coenzyme Q10 deficiency
- Cohen Syndrome
- Colon cancer
- Colorblind
- Colorectal cancer
- Combined partial 17-alpha-hydroxylase/17
- Complete combined 17-alpha-hydroxylase/17
- Conduct disorder
- Cone-rod dystrophy 7
- Congenital adrenal hyperplasia
- Congenital contractural arachnodactyly
- Congenital disorder of glycosylation
- Congenital erythropoietic porphyria
- Congenital long QT syndrome
- Congenital myasthenic syndrome
- Corneal dystrophy
- Cornelia de Lange syndrome 1
- Coronary artery calcification
- Coronary artery disease
- Coronary artery spasm 3
- Cowden syndrome 1
- Crigler-Najjar syndrome
- Crohn's disease
- Cushing's syndrome
- Cyclosporine response - Dosage
- Cystic Fibrosis
D
E
F
- Fabry disease
- Factor VII Marburg I Variant Thrombophilia
- Factor XI deficiency
- Familial colorectal cancer
- Familial dysautonomia
- Familial exudative vitreoretinopathy
- Familial hyperaldosteronism
- Familial hypercholesterolemia
- Familial hyperlipoproteinemia
- Familial hypertrophic cardiomyopathy
- Familial Mediterranean Fever
- Familial type 3 hyperlipoproteinemia
- Familial X-linked hypophosphatemic vitamin D refractory rickets
- Fanconi anemia
- Fatal familial insomnia
- Female Infertility
- Fentanyl response - Dosage
- Fetal alcohol syndrome
- Fibrodysplasia ossificans progressiva
- Fibromyalgia
