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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