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(400 entries max)
Category - Disease (KW-9995)
Keywords navigation
›AIDS
›Albinism
›Allergen
›Alport syndrome
›Alzheimer disease
More »
›Albinism
›Allergen
›Alport syndrome
›Alzheimer disease
More »
›Ectodermal dysplasia
›Tumor suppressor
›Atherosclerosis
›Autoimmune encephalomyelitis
›Autoimmune uveitis
›Bernard Soulier syndrome
›Cardiomyopathy
›Chronic granulomatous disease
›Cockayne syndrome
›Cone-rod dystrophy
›Crown gall tumor
›Cystinuria
›Deafness
›Dental caries
›Diabetes insipidus
›Diabetes mellitus
›Disease variant
›Down syndrome
›Dwarfism
›Ehlers-Danlos syndrome
›Epidermolysis bullosa
›Gaucher disease
›Glutaricaciduria
›Glycogen storage disease
›Gangliosidosis
›Gout
›Hemophilia
›Hereditary hemolytic anemia
›Hereditary multiple exostoses
›Hereditary nonpolyposis colorectal cancer
›Hirschsprung disease
›Holoprosencephaly
›Hyperlipidemia
›Li-Fraumeni syndrome
›Lissencephaly
›Long QT syndrome
›Malaria
›Maple syrup urine disease
›Mucopolysaccharidosis
›Neurodegeneration
›Obesity
›Oncogene
›Phenylketonuria
›Neuropathy
›Proto-oncogene
›Pseudohermaphroditism
›Retinitis pigmentosa
›Rhizomelic chondrodysplasia punctata
›SCID
›Stargardt disease
›Stickler syndrome
›Systemic lupus erythematosus
›Thrombophilia
›Trypanosomiasis
›von Willebrand disease
›Whooping cough
›Williams-Beuren syndrome
›Xeroderma pigmentosum
›Epilepsy
›Cataract
›Congenital disorder of glycosylation
›Leber congenital amaurosis
›Primary microcephaly
›Parkinson disease
›Parkinsonism
›Bartter syndrome
›Congenital muscular dystrophy
›Age-related macular degeneration
›Fanconi anemia
›Short QT syndrome
›Mucolipidosis
›Limb-girdle muscular dystrophy
›Aicardi-Goutieres syndrome
›Familial hemophagocytic lymphohistiocytosis
›Congenital adrenal hyperplasia
›Glaucoma
›Kallmann syndrome
›Peroxisome biogenesis disorder
›Atrial septal defect
›Ichthyosis
›Primary hypomagnesemia
›Nephronophthisis
›Congenital hypothyroidism
›Congenital erythrocytosis
›Amelogenesis imperfecta
›Osteopetrosis
›Intrahepatic cholestasis
›Craniosynostosis
›Mental retardation
›Brugada syndrome
›Aortic aneurysm
›Congenital myasthenic syndrome
›Palmoplantar keratoderma
›Amyloidosis
›Dyskeratosis congenita
›Microphthalmia
›Congenital stationary night blindness
›Hypogonadotropic hypogonadism
›Atrial fibrillation
›Pontocerebellar hypoplasia
›Congenital generalized lipodystrophy
›Dystonia
›Diamond-Blackfan anemia
›Leukodystrophy
›Niemann-Pick disease
›Heterotaxy
›Nemaline myopathy
›Asthma
›Peters anomaly
›Myofibrillar myopathy
›Cushing syndrome
›Hypotrichosis
›Osteogenesis imperfecta
›Premature ovarian failure
›Emery-Dreifuss muscular dystrophy
›Hemolytic uremic syndrome
›Ciliopathy
›Schizophrenia
›Corneal dystrophy
›Dystroglycanopathy
›Autism spectrum disorder
›Primary mitochondrial disease
« Less›Tumor suppressor
›Atherosclerosis
›Autoimmune encephalomyelitis
›Autoimmune uveitis
›Bernard Soulier syndrome
›Cardiomyopathy
›Chronic granulomatous disease
›Cockayne syndrome
›Cone-rod dystrophy
›Crown gall tumor
›Cystinuria
›Deafness
›Dental caries
›Diabetes insipidus
›Diabetes mellitus
›Disease variant
›Down syndrome
›Dwarfism
›Ehlers-Danlos syndrome
›Epidermolysis bullosa
›Gaucher disease
›Glutaricaciduria
›Glycogen storage disease
›Gangliosidosis
›Gout
›Hemophilia
›Hereditary hemolytic anemia
›Hereditary multiple exostoses
›Hereditary nonpolyposis colorectal cancer
›Hirschsprung disease
›Holoprosencephaly
›Hyperlipidemia
›Li-Fraumeni syndrome
›Lissencephaly
›Long QT syndrome
›Malaria
›Maple syrup urine disease
›Mucopolysaccharidosis
›Neurodegeneration
›Obesity
›Oncogene
›Phenylketonuria
›Neuropathy
›Proto-oncogene
›Pseudohermaphroditism
›Retinitis pigmentosa
›Rhizomelic chondrodysplasia punctata
›SCID
›Stargardt disease
›Stickler syndrome
›Systemic lupus erythematosus
›Thrombophilia
›Trypanosomiasis
›von Willebrand disease
›Whooping cough
›Williams-Beuren syndrome
›Xeroderma pigmentosum
›Epilepsy
›Cataract
›Congenital disorder of glycosylation
›Leber congenital amaurosis
›Primary microcephaly
›Parkinson disease
›Parkinsonism
›Bartter syndrome
›Congenital muscular dystrophy
›Age-related macular degeneration
›Fanconi anemia
›Short QT syndrome
›Mucolipidosis
›Limb-girdle muscular dystrophy
›Aicardi-Goutieres syndrome
›Familial hemophagocytic lymphohistiocytosis
›Congenital adrenal hyperplasia
›Glaucoma
›Kallmann syndrome
›Peroxisome biogenesis disorder
›Atrial septal defect
›Ichthyosis
›Primary hypomagnesemia
›Nephronophthisis
›Congenital hypothyroidism
›Congenital erythrocytosis
›Amelogenesis imperfecta
›Osteopetrosis
›Intrahepatic cholestasis
›Craniosynostosis
›Mental retardation
›Brugada syndrome
›Aortic aneurysm
›Congenital myasthenic syndrome
›Palmoplantar keratoderma
›Amyloidosis
›Dyskeratosis congenita
›Microphthalmia
›Congenital stationary night blindness
›Hypogonadotropic hypogonadism
›Atrial fibrillation
›Pontocerebellar hypoplasia
›Congenital generalized lipodystrophy
›Dystonia
›Diamond-Blackfan anemia
›Leukodystrophy
›Niemann-Pick disease
›Heterotaxy
›Nemaline myopathy
›Asthma
›Peters anomaly
›Myofibrillar myopathy
›Cushing syndrome
›Hypotrichosis
›Osteogenesis imperfecta
›Premature ovarian failure
›Emery-Dreifuss muscular dystrophy
›Hemolytic uremic syndrome
›Ciliopathy
›Schizophrenia
›Corneal dystrophy
›Dystroglycanopathy
›Autism spectrum disorder
›Primary mitochondrial disease
Definition
Keywords assigned to proteins because they are involved in a specific disease.
