Atlas Médico

Accessible medical knowledge

All Diseases

Autoimmune atherosclerosis

Autoimmune autonomic ganglionopathy

Autoimmune bullous skin disease

Autoimmune cardiomyopathy

Autoimmune cholangitis

Autoimmune disease

Autoimmune disease of ear, nose and throat

Autoimmune disease, multisystem, infantile-onset, 2

Autoimmune disorder of blood

Autoimmune disorder of cardiovascular system

Autoimmune disorder of central nervous system

Autoimmune disorder of endocrine system

Autoimmune disorder of exocrine system

Autoimmune disorder of gastrointestinal tract

Autoimmune disorder of musculoskeletal system

Autoimmune disorder of peripheral nervous system

Autoimmune disorder of the nervous system

Autoimmune encephalitis

Autoimmune encephalopathy with parasomnia and obstructive sleep apnea

Autoimmune enteropathy

Autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome

Autoimmune epilepsy

Autoimmune gastritis

Autoimmune glomerulonephritis

Autoimmune hemolytic anemia

Autoimmune hemolytic anemia, cold type

Autoimmune hemolytic anemia, warm type

Autoimmune hepatitis

Autoimmune

Autoimmune hepatitis type 1

Autoimmune hepatitis type 2

Autoimmune hepatitis type 3

Autoimmune hypoparathyroidism

Autoimmune inner ear disease

Autoimmune interstitial lung disease-arthritis syndrome

Autoimmune limbic encephalitis

Autoimmune lymphoproliferative syndrome

Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency

Autoimmune lymphoproliferative syndrome type 2A

Autoimmune lymphoproliferative syndrome type 2B

Autoimmune lymphoproliferative syndrome type 4

Autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD

Autoimmune myocarditis

Autoimmune neuropathy

Autoimmune oophoritis

Autoimmune optic neuritis

Autoimmune pancreatitis

Autoimmune pancreatitis type 1

Autoimmune pancreatitis type 2

Autoimmune polyendocrine syndrome type 1

Autoimmune polyendocrinopathy

Autoimmune polyendocrinopathy type 2

Autoimmune polyendocrinopathy type 3

Autoimmune primary ovarian failure

Autoimmune pulmonary alveolar proteinosis

Autoimmune pulmonary disease due to PD-1 deficiency

Autoimmune retinopathy

Autoimmune thrombocytopenia

Autoimmune thrombocytopenic purpura

Autoimmune thyroid disease

Autoimmune urticaria

Autoimmune uveitis

Autoimmune vasculitis

Autoinflammatory disease, X-linked

Autoinflammatory syndrome

Autoinflammatory syndrome due to TBK1 deficiency

Autoinflammatory syndrome with immunodeficiency

Autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency

Autonomic dysreflexia

Autonomic nervous system disorder

Autonomic nervous system neoplasm

Autonomic neuropathy

Autosomal agammaglobulinemia

Autosomal anomaly

Autosomal dominant Alport syndrome

Autosomal dominant auditory neuropathy 1

Autosomal dominant brachyolmia

Autosomal dominant cataract

Autosomal dominant centronuclear myopathy

Autosomal dominant cerebellar ataxia

Autosomal dominant cerebellar ataxia type I

Autosomal dominant cerebellar ataxia type III

Autosomal dominant cerebellar ataxia, deafness and narcolepsy

Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation

Autosomal dominant Charcot-Marie-Tooth disease type 2K

Autosomal dominant Charcot-Marie-Tooth disease type 2M

Autosomal dominant Charcot-Marie-Tooth disease type 2W

Autosomal dominant chondrodysplasia punctata

Autosomal dominant coarctation of aorta

Autosomal dominant complex spastic paraplegia

Autosomal dominant cutis laxa

Autosomal dominant deafness - onychodystrophy syndrome

Autosomal dominant disease

Autosomal dominant distal myopathy

Autosomal dominant distal renal tubular acidosis

Autosomal dominant dopa-responsive dystonia

Autosomal dominant Ehlers-Danlos syndrome, vascular type

Autosomal dominant Emery-Dreifuss muscular dystrophy

Autosomal dominant epilepsy with auditory features

Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome

Autosomal dominant hyperinsulinism due to Kir6.2 deficiency