Products by Disease or Condition
MyBioSource's team have spent countless hours of research to find the most common diseases or conditions and associate them with our products.
Each disease or condition is linked to the top products based on our sophisticated "P2D (Products2Disease)" indexing algorithm.
- A
- Aarskog Syndrome
- AAT deficiency
- Abdominal Neoplasms
- Abdominal Pain
- Aberrant Crypt Foci
- Abetalipoproteinemia
- Abnormalities, Drug-Induced
- Abnormalities, Multiple
- Abortion, Habitual
- Abortion, Spontaneous
- Abortion, Threatened
- Abortion, Veterinary
- Absent corpus callosum cataract immunodeficiency
- Absent radii and thrombocytopenia
- Achalasia Addisonianism Alacrimia syndrome
- Acheiropodia
- Achondrogenesis type 1A
- Achondrogenesis type 1B
- Achondroplasia
- Achromatopsia 2
- Achromatopsia 3
- Acidosis
- Acidosis, Lactic
- Acidosis, Renal Tubular
- Acidosis, Respiratory
- Acne Vulgaris
- Acquired angioedema
- Acquired Immunodeficiency Syndrome
- Acro-Osteolysis
- Acrocallosal Syndrome
- Acrocephalopolysyndactyly Type II
- Acrocephalosyndactylia
- Acrodermatitis
- Acrodermatitis enteropathica
- ACROKERATOSIS VERRUCIFORMIS
- Acromegaly
- Acromesomelic dysplasia, Maroteaux type
- Acromicric dysplasia
- ACTH Deficiency, Isolated
- ACTH-Secreting Pituitary Adenoma
- Acute Coronary Syndrome
- Acute Disease
- Acute Kidney Injury
- Acute Lung Injury
- Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of
- ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF
- ACYL-CoA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF
- Addison Disease
- Adenocarcinoma
- Adenocarcinoma of lung
- Adenocarcinoma, Bronchiolo-Alveolar
- Adenocarcinoma, Papillary
- Adenoma
- Adenoma, Islet Cell
- Adenoma, Liver Cell
- Adenoma, Oxyphilic
- Adenomatous Polyposis Coli
- Adenomatous Polyps
- Adenosine monophosphate deaminase deficiency
- Adenoviridae Infections
- Adenylate Kinase Deficiency, Hemolytic Anemia Due To
- Adenylosuccinate lyase deficiency
- Adrenal Cortex Diseases
- Adrenal Cortex Neoplasms
- Adrenal Gland Diseases
- Adrenal Gland Neoplasms
- Adrenal Hyperplasia, Congenital
- ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY
- ADRENAL HYPOPLASIA, CONGENITAL
- Adrenal Insufficiency
- Adrenocortical Adenoma
- Adrenocortical Carcinoma
- Adrenocortical Hyperfunction
- Adrenocorticotropic hormone deficiency
- Adrenoleukodystrophy
- ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM
- Adult-onset citrullinemia type 2
- Advanced Sleep-Phase Syndrome, Familial
- Affective Disorders, Psychotic
- Afibrinogenemia
- Afibrinogenemia congenital
- Agammaglobulinemia
- AGAMMAGLOBULINEMIA, X-LINKED
- Aggressive Periodontitis
- Aging, Premature
- Agranulocytosis
- AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY
- Aicardi-Goutieres syndrome
- Aicardi-Goutieres Syndrome 3
- Aicardi-Goutieres Syndrome 4
- Aicardi-Goutieres syndrome 5
- AIDS-Related Opportunistic Infections
- Airway Obstruction
- Alagille Syndrome
- ALAND ISLAND EYE DISEASE
- ALBINISM, OCULOCUTANEOUS, TYPE IV
- Albright's hereditary osteodystrophy
- Albuminuria
- Alcohol Withdrawal Seizures
- Alcohol-Induced Disorders
- Alcohol-Induced Disorders, Nervous System
- Alcohol-Related Disorders
- Alcoholic Intoxication
- Alcoholism
- Alexander Disease
- Alkalosis
- Alkaptonuria
- Allan-Herndon-Dudley syndrome
- ALLERGIC RHINITIS
- Alopecia
- Alopecia Areata
- alpha 1-Antitrypsin Deficiency
- Alpha-2-plasmin inhibitor deficiency
- alpha-Mannosidosis
- alpha-Thalassemia
- Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis
- Alport syndrome, recessive type
- ALPORT SYNDROME, X-LINKED
- Alstrom Syndrome
- Alternating hemiplegia of childhood
- Alveolar Bone Loss
- Alveolar capillary dysplasia
- Alzheimer Disease
- Alzheimer disease type 4
- Amaurosis hypertrichosis
- Amblyopia
- Amelogenesis Imperfecta
- Amelogenesis Imperfecta, Hypomaturation Type, Iia2
- Amelogenesis Imperfecta, Hypomaturation Type, Iia3
- Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 1
- Amenorrhea
- Amino Acid Metabolism, Inborn Errors
- Aminoacylase 1 deficiency
- Amish lethal microcephaly
- Amnesia
- Amphetamine-Related Disorders
- Amyloid Neuropathies, Familial
- Amyloidosis
- Amyloidosis, Familial
- AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1
- Amyotrophic Lateral Sclerosis
- Amyotrophic Lateral Sclerosis 10
- Amyotrophic Lateral Sclerosis 11
- Amyotrophic Lateral Sclerosis 2, Juvenile
- AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE
- Amyotrophic Lateral Sclerosis 8
- AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1
- AMYOTROPHY, HEREDITARY NEURALGIC
- Andersen Syndrome
- Anemia
- Anemia, Aplastic
- Anemia, Diamond-Blackfan
- Anemia, Diamond-Blackfan, 3
- ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE I
- ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE II
- Anemia, Dyserythropoietic, Congenital
- Anemia, Hemolytic
- Anemia, Hemolytic, Autoimmune
- Anemia, Hemolytic, Congenital
- Anemia, Hemolytic, Congenital Nonspherocytic
- Anemia, Hypochromic
- ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD
- Anemia, Iron-Deficiency
- Anemia, Macrocytic
- Anemia, Megaloblastic
- Anemia, Sickle Cell
- Anemia, Sideroblastic
- Anemia, sideroblastic spinocerebellar ataxia
- ANEMIA, SIDEROBLASTIC, PYRIDOXINE-REFRACTORY, AUTOSOMAL RECESSIVE
- Aneuploidy
- Aneurysm
- Aneurysm, Dissecting
- Angelman Syndrome
- Angina Pectoris
- Angina, Unstable
- Angioedema
- Angioedemas, Hereditary
- Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps
- Aniridia
- Anodontia
- Anonychia congenita
- Anophthalmia with pulmonary hypoplasia
- Anophthalmos
- Anorexia
- Anotia
- Anoxia
- Anterior segment mesenchymal dysgenesis
- Antisocial Personality Disorder
- Antithrombin III Deficiency
- ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS
- Anus, Imperforate
- Anxiety Disorders
- Aortic Aneurysm
- Aortic Aneurysm, Abdominal
- Aortic Aneurysm, Thoracic
- Aortic Diseases
- Aortic Rupture
- Aortic Stenosis, Supravalvular
- Aortic Valve Stenosis
- Aphasia
- Apnea
- Apparent mineralocorticoid excess
- Apraxias
- Arachnodactyly
- Arginine:Glycine Amidinotransferase Deficiency
- Arrest of spermatogenesis
- Arrhythmia, Sinus
- Arrhythmias, Cardiac
- Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
- Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
- Arrhythmogenic Right Ventricular Dysplasia, Familial, 5
- Arrhythmogenic Right Ventricular Dysplasia, Familial, 9
- Arsenic Poisoning
- Arterial calcification of infancy
- Arterial Occlusive Diseases
- Arterial Tortuosity Syndrome
- Arteriosclerosis
- Arteriovenous Malformations
- Arteritis
- Arthralgia
- Arthritis
- Arthritis, Experimental
- Arthritis, Gouty
- Arthritis, Psoriatic
- Arthritis, Reactive
- Arthritis, Rheumatoid
- Arthrogryposis
- Arthrogryposis renal dysfunction cholestasis syndrome
- Arthropathy, progressive pseudorheumatoid, of childhood
- Arts syndrome
- Ascites
- Ascorbic Acid Deficiency
- Asperger Syndrome
- Asphyxia
- ASPHYXIATING THORACIC DYSTROPHY 2
- ASPHYXIATING THORACIC DYSTROPHY 3
- Asthenozoospermia
- Asthma
- Asthma, Aspirin-Induced
- Asthma, Exercise-Induced
- ASTHMA, NASAL POLYPS, AND ASPIRIN INTOLERANCE
- Asthma, Occupational
- ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1
- Astigmatism
- Astrocytoma
- Ataxia
- Ataxia Telangiectasia
- ATAXIA-TELANGIECTASIA-LIKE DISORDER
- ATAXIA-TELANGIECTASIA-LIKE DISORDER 1
- Atelosteogenesis type 2
- ATELOSTEOGENESIS, TYPE III
- Atherosclerosis
- Athetosis
- ATR-X syndrome
- Atrial Fibrillation
- Atrial Fibrillation, Familial, 7
- Atrial Flutter
- Atrial Septal Defect 6
- ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS
- Atrioventricular Block
- Atrophy
- Attention Deficit and Disruptive Behavior Disorders
- Attention Deficit Disorder with Hyperactivity
- Atypical hemolytic uremic syndrome
- Auditory Neuropathy, Autosomal Dominant, 1
- Auditory Perceptual Disorders
- AUTISM, SUSCEPTIBILITY TO, X-LINKED 1
- Autistic Disorder
- AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1
- Autoimmune Diseases
- Autoimmune polyendocrinopathy syndrome, type 1
- Autonomic Nervous System Diseases
- Autosomal dominant distal renal tubular acidosis
- AXENFELD-RIEGER SYNDROME, TYPE 1
- AXENFELD-RIEGER SYNDROME, TYPE 3
- Azoospermia