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Disease

Search Disease Categories by Alphabetical Order:

A B C D E F G H I J K L M N O P Q R S T U V W Y Z 

 

A

• Age-related macular degeneration • Aicardi-Goutieres syndrome
• AIDS • Albinism
• Allergen • Alport syndrome
• Alzheimer disease • Amelogenesis imperfecta
• Amyloidosis • Amyotrophic lateral sclerosis
• Aortic aneurysm • Asthma
• Atherosclerosis • Atrial fibrillation
• Atrial septal defect • Autoimmune encephalomyelitis

 

B

• Bardet-Biedl syndrome • Bartter syndrome
• Bernard Soulier syndrome • Brugada syndrome

 

C

• Cardiomyopathy • Cataract
• Charcot-Marie-Tooth disease • Chronic granulomatous disease
• Ciliopathy • Cockayne syndrome
• Cone-rod dystrophy • Congenital adrenal hyperplasia
• Congenital disorder of glycosylation • Congenital dyserythropoietic anemia
• Congenital erythrocytosis • Congenital generalized lipodystrophy
• Congenital hypothyroidism • Congenital muscular dystrophy
• Congenital myasthenic syndrome • Congenital stationary night blindness
• Craniosynostosis • Cushing syndrome
• Cystinuria

 

D

• Deafness • Dejerine-Sottas syndrome
• Desmin-related myopathy • Diabetes insipidus
• Diabetes mellitus • Diamond-Blackfan anemia
• Disease mutation • Dwarfism
• Dyskeratosis congenita • Dystonia

 

E

• Ectodermal dysplasia • Ehlers-Danlos syndrome
• Elliptocytosis • Emery-Dreifuss muscular dystrophy
• Epidermolysis bullosa • Epilepsy

 

F

• Familial hemophagocytic lymphohistiocytosis • Fanconi anemia

 

G

• Gangliosidosis • Gaucher disease
• Glaucoma • Glutaricaciduria
• Glycogen storage disease • Gout

 

H

• Hemolytic uremic syndrome • Hemophilia
• Hereditary hemolytic anemia • Hereditary multiple exostoses
• Hereditary nonpolyposis colorectal cancer • Hereditary spastic paraplegia
• Hermansky-Pudlak syndrome • Heterotaxy
• Hirschsprung disease • Holoprosencephaly
• Hyperlipidemia • Hypogonadotropic hypogonadism
• Hypotrichosis

 

I

• Ichthyosis Gene Trends And Antibodies • Intrahepatic Cholestasis Gene Trends And Antibodies

 

J

• Joubert Syndrome Gene Trends And Antibodies

 

K

• Kallmann syndrome • Kartagener syndrome

 

L

• Lacrimo-auriculo-dento-digital syndrome • Leber congenital amaurosis
• Leber hereditary optic neuropathy • Leigh syndrome
• Leukodystrophy • Li-Fraumeni syndrome
• Limb-girdle muscular dystrophy • Lissencephaly
• Long QT syndrome

 

M

• Malaria • Maple syrup urine disease
• Meckel syndrome • MELAS syndrome
• Mental retardation • Metachromatic leukodystrophy
• Microphthalmia • Mucolipidosis
• Mucopolysaccharidosis • Myofibrillar myopathy

 

N

• Nemaline myopathy • Nephronophthisis
• Neurodegeneration • Neuronal ceroid lipofuscinosis
• Neuropathy • Niemann-Pick disease
• Non-syndromic deafness

 

O

• Obesity • Oncogene
• Osteogenesis imperfecta • Osteopetrosis

 

P

• Palmoplantar keratoderma • Parkinson disease
• Parkinsonism • Peroxisome biogenesis disorder
• Peters anomaly • Phenylketonuria
• Pontocerebellar hypoplasia • Premature ovarian failure
• Primary ciliary dyskinesia • Primary hypomagnesemia
• Primary microcephaly • Progressive external ophthalmoplegia
• Proto-oncogene • Pseudohermaphroditism
• Pyropoikilocytosis

 

R

• Retinitis pigmentosa • Rhizomelic chondrodysplasia punctata
• RuleBase RU003304

 

S

• SCID • Senior-Loken syndrome
• Short QT syndrome • Spinocerebellar ataxia
• Stargardt disease • Stickler syndrome
• Systemic lupus erythematosus

 

T

• Thrombophilia • Tumor suppressor

 

U

• Usher syndrome

 

V

• von Willebrand disease

 

W

• Waardenburg syndrome • Whooping cough
• Williams-Beuren syndrome

 

X

• Xeroderma Pigmentosum Gene Trends And Antibodies

 

Z

• Zellweger syndrome