A Diseases
From Anvita Health Wiki
Introduction
- A2 (aortic valve heart sound)
- AA amyloidosis
- Aaland island eye disease
- Aarskog-Scott syndrome
- ABCD syndrome
- abdominal aortic aneurysm
- abdominal compartment syndrome
- abdominal pain
- abdominal trauma
- abetalipoproteinemia
- abnormal grief
- Abnormal Hepatic Function Test
- Abnormal Liver Function Study
- Abnormal Liver Function Test
- Abnormal Loss of Weight
- abnormal serum Transaminase or serum LDH
- abnormal thyroid hormone metabolism
- abnormality of gait
- abrasion
- abruptio placentae
- absence epilepsy type 2
- absence epilepsy type 3
- absence epilepsy type 4
- absence of ulna & fibula with severe limb deficiency
- absence seizure
- absolute scotoma
- absorptive hypercalciuria
- abulia
- acalculia
- acanthocytosis
- acantholysis
- acanthosis nigricans
- accelerated idioventricular rhythm
- acetaminophen poisoning
- achalasia
- achalasia-addisonianism-alacrima syndrome
- Achilles tendon rupture
- Achilles tendonitis
- achlorhydria
- achondrogenesis
- achondrogenesis type 1B
- achondroplasia
- achromatopsia
- achromatopsia 2
- achromatopsia 3
- acid-base disorder
- acidosis
- acne
- acoustic neuroma
- acoustic trauma
- acquired epileptiform aphasia
- acquired idiopathic sideroblastic anemia
- Acquired Immuno-Deficiency Syndrome
- acquired platelet aggregation disorder
- acquired polycystic kidney disease
- acral erythema
- acral fibromyxoma
- acral lentiginous melanoma
- acro-dermato-ungual-acrimal-tooth syndrome
- acrobrachycephaly
- acrocallosal syndrome
- acrocapitofemoral dysplasia
- acrocephalopolysyndactyly
- acrocephalopolysyndactyly type 2
- acrocephalosyndactyly type I
- acrocephalosyndactyly type III
- acrocephalosyndactyly type V
- acrochordon
- acrocyanosis
- acrodermatitis enteropathica
- acrokeratosis paraneoplastica
- acromegaly
- acromesomelic chondrodysplasia
- acromesomelic chondrodysplasia Grebe type
- acromesomelic chondrodysplasia Hunter-Thompson type
- ACTH deficiency
- ACTH-independent macronodular adrenal hyperplasia
- actinic cheilitis
- actinic keratosis
- actinic prurigo
- actinic purpura
- actinomycosis
- activated protein C resistance
- acute adrenal insufficiency
- acute angle-closure glaucoma
- acute aortic syndrome
- acute arterial occlusion
- acute basophilic leukemia
- acute coronary arterial thrombosis
- acute coronary syndrome
- acute diarrhea
- acute disseminated encephalomyelitis
- acute eosinophilic leukemia
- acute eosinophilic pneumonia
- acute erythroblastic leukemia
- acute febrile neutrophilic dermatosis
- acute functional psychosis
- acute glomerulonephritis
- acute heart failure
- acute hypersensitivity pneumonitis
- acute infantile liver failure
- acute intermittent porphyria
- acute interstitial nephritis
- acute leukemia
- acute leukocytoclastic vasculitis
- acute liver failure
- acute lung injury
- acute lymphoblastic leukemia
- acute lymphoblastic leukemia with lymphomatous features
- acute lymphoblastic leukemia, L3
- acute megakaryoblastic leukemia
- acute mitral regurgitation
- acute monocytic leukemia
- acute mountain sickness
- acute myeloblastic leukemia minimally differentiated
- acute myeloblastic leukemia without maturation
- acute myeloid leukemia
- acute myeloid leukemia 11q23
- acute myeloid leukemia therapy related
- acute myeloid leukemia t[16;16][p13;q22]
- acute myeloid leukemia t[18 21][q22 q22]
- acute myelomonocytic leukemia
- acute myelomonocytic leukemia/AML-M4Eos
- acute necrotizing ulcerative gingivitis
- acute otitis media
- acute pain
- acute pancreatitis
- acute panmyelosis with myelofibrosis
- acute promyelocytic leukemia
- acute recurrent rhabdomyolysis
- acute renal cortical necrosis
- acute renal failure
- acute renal failure in malignancy
- acute renal failure in pregnancy
- acute respiratory distress syndrome
- acute respiratory failure
- acute retroviral syndrome
- acute sickle cell chest syndrome
- acute silicosis
- acute sinusitis
- acute splenic sequestration crisis
- acute tubular necrosis
- acute urethral syndrome
- acute uric acid nephropathy
- acyl-CoA dehydrogenase family member type 9 deficiency
- addiction
- Addison's disease
- Addisonian crisis
- ADEM
- adenocarcinoma
- adenocarcinoma of the breast
- adenocarcinoma of the colon
- adenocarcinoma of the lung
- adenocarcinoma of the ovary
- adenocarcinoma of the prostate
- adenocarcinoma, pancreas
- adenohypophysitis
- adenoma
- adenoma of the liver
- adenomatous polyposis coli
- adenopathy
- adenosine deaminase deficiency
- ADHD (attention deficit hyperactivity disorder)
- adhesive capsulitis
- adiaphoresis
- Adie syndrome
- adipocyte neoplasm
- adipositas dolorosa
- adjustment disorder
- adnexal cyst
- adrenal cortical adenoma
- adrenal cortical carcinoma
- adrenal cortical hyperplasia
- adrenal hemorrhage
- adrenal hyperplasia 1
- adrenal hyperplasia type 2
- adrenal incidentaloma
- adrenal insufficiency
- adrenal neoplasm
- adrenalitis
- adrenocortical hyperplasia
- adrenocortical insufficiency without ovarian defect
- adrenogenital syndrome
- adrenoleukodystrophy pseudoneonatal
- Adson's sign
- adult granulosa cell tumor
- adult polycystic kidney disease
- adult polyglucosan body disease
- adult t cell lymphoma leukemia
- advanced sleep-phase syndrome
- adverse drug effect
- adverse drug effects in the elderly
- aerophagia
- agammaglobulinemia
- aganglionic megacolon
- age-associated changes in hearing
- age-associated memory impairment
- age-related endocrinopathy
- agenesis of the corpus callosum with abnormal genitalia
- agenesis of the corpus callosum with peripheral neuropathy
- aggression
- agitation
- agitation & psychosis in the elderly
- agnogenic myeloid metaplasia
- agnosia
- agranulocytosis
- agraphia
- agyria
- AICA-ribosuria
- Aicardi syndrome
- Aicardi-Goutieres syndrome
- AIDS
- AIDS dementia complex
- AIDS in children
- AIDS-associated anemia
- AIDS-associated dermatologic disorder
- AIDS-associated neutropenia
- AIDS-associated opportunistic infection
- AIDS-induced thrombocytopenia
- air embolism
- airway obstruction
- AK (actinic keratosis)
- akathisia
- akinetic mutism
- AL amyloidosis
- alacrima
- Alagille syndrome
- alastrim
- Albers-Schonberg disease
- albinism, partial
- albopapuloid dominant dystrophic epidermolysis bullosa
- Albrectsen-Svendsen syndrome
- Albright's hereditary osteodystrophy
- albuminuria
- alcohol intoxication
- alcohol withdrawal seizure
- alcohol withdrawal syndrome
- alcohol-associated dementia
- alcohol-responsive dystonia
- alcoholic cirrhosis
- alcoholic hangover
- alcoholic hepatitis
- alcoholic liver disease
- alcoholism
- aldosterone deficiency 1
- aldosterone deficiency 2
- aldosteronoma
- Alexander's leukodystrophy
- alexia
- alkaptonuria
- ALL (acute lymphoblastic leukemia)
- allergic angiitis & granulomatosis of Churg-Strauss
- allergic bronchopulmonary aspergillosis
- allergic contact dermatitis
- allergic coryza
- allergic pneumonitis
- allergic rhinitis
- allergic rhinoconjunctivitis
- allergy
- allergy to cow's milk
- Allgrove syndrome
- allodynia
- alopecia
- alopecia areata
- alopecia universalis congenita
- alopecia universalis congenita Mari type
- Alper's disease
- Alpers-Huttenlocher syndrome
- alpha thalassemia
- alpha thalassemia 1
- alpha thalassemia 2
- alpha thalassemia-0
- alpha-1 antitrypsin deficiency
- alpha-2-antiplasmin deficiency
- alpha-chain disease
- alpha-methylacetoaceticaciduria
- alpha-methylacyl-CoA racemase deficiency
- alpha-thalassemia myelodysplasia syndrome
- Alport syndrome
- Alport syndrome with mental retardation midface hypoplasia & elliptocytosis
- ALS-parkinsonism-dementia complex
- Alstrom syndrome
- altered mental status
- altered state of consciousness
- alternating hemiplegia
- altitudinal hemianopia
- aluminum osteodystrophy
- aluminum toxicity
- alveolar capillary dysplasia
- alveolar cell carcinoma
- alveolar hemorrhage
- alveolar proteinosis
- alveolar rhabdomyosarcoma
- alveolar soft part sarcoma
- Alzheimer's disease
- Alzheimer's disease, early-onset
- Alzheimer's disease, Lewy body variant
- AMACR deficiency
- amaurosis fugax
- amblyopia
- amebiasis
- amelogenesis imperfecta
- amelogenesis imperfecta hypoplastic type 1
- amelogenesis imperfecta hypoplastic type 1B
- amelogenesis imperfecta type 1C
- amelogenesis imperfecta type 2A1
- amelogenesis imperfecta type 4
- amenorrhea
- amine precursor uptake & decarboxylation tumor
- aminoacylase-1 deficiency
- aminoglycoside-induced deafness
- aminolevulinate dehydratase deficiency pophyria
- Amish infantile epilepsy syndrome
- Amish lethal microcephaly
- Amish nemaline myopathy
- AML (acute myeloid leukemia)
- AML gene expression profiling clusters
- AMME complex
- amnesia
- amnesic psychosis
- amnesic-dysnomic aphasia
- amniotic fluid embolism
- AMP deaminase deficiency
- ampulla of Vater adenocarcinoma
- amyloidosis
- amyloidosis type 5
- amyloidosis type 8
- amyopathic dermatomyositis
- amyotrophic lateral sclerosis
- amyotrophy dementia parkinsonism
- anaerobic cellulitis
- anaerobic infection
- anagen effluvium
- anal fissure
- anal incontinence
- anal pruritis
- analgesic nephropathy
- analgesic rebound headache
- analphalipoproteinemia
- anaphylactoid reaction
- anaphylaxis
- anaplasmosis
- anaplastic astrocytoma
- anaplastic ependymoma
- anaplastic large cell lymphoma t cell type
- anaplastic meningioma
- anaplastic oligodendroglioma
- anaplastic thyroid carcinoma
- Andersen cardiodysrhythmic periodic paralysis
- Anderson disease
- Anderson type glycogen storage disease
- androgen excess
- androgen insensitivity
- androgen insufficiency
- androgenic alopecia
- andropause
- anemia
- anemia associated with iron deficiency
- anemia in pregnancy
- anemia of chronic disease
- anemia of chronic inflammation
- anemia of chronic liver disease
- anemia of endocrine failure
- anemia of renal failure
- anemia, sideroblastic acquired idiopathic
- Angelman syndrome
- angina
- angioblastoma
- angiocentric lymphoma
- angiodysplasia
- angioedema
- angiofibroma
- angiofollicular lymph node hyperplasia
- angiographically significant CAD
- angioimmunoblastic t cell lymphoma
- angiokeratoma corporis diffusum
- angiokeratoma of Fordyce
- angiokeratoma of Mibelli
- angiomatoid fibrous histiocytoma
- angiomatous nevus
- angiomyolipoma
- angiostrongylosis
- angular cheilitis
- angular gyrus syndrome
- angular stomatitis
- anhidrosis
- anhidrotic ectodermal dysplasia
- anhidrotic ectodermal dysplasia with cleft lip/palate
- animal spongiform encephalopathy
- aniridia type 2
- anisakiasis
- aniseikonia
- anisocoria
- anisometropia
- ankle pain
- ankle sprain
- ankle-brachial index
- ankloglossia
- ankyloglossia
- ankylosing spondylitis
- ankylosis
- ankylostoma
- anogenital wart
- anomic aphasia
- anophthalmia with associated anomalies
- anorchia
- anorectal fistula
- anorectal pain
- anorectal syndrome
- anorexia nervosa
- anosmia
- anterior cingulate syndrome
- anterior segment mesenchymal dysgenesis
- anterior segment ocular dysgenesis
- anterior uveitis
- anterolisthesis
- anthrax
- anti GQ1b antibody syndrome
- anti-glomerular basement membrane disease
- antibiotic side effects in the elderly
- anticholinesterase toxicity
- antiphospholipid syndrome
- antisocial personality disorder
- antithrombin deficiency
- Antley-Bixler syndrome
- anuria
- anxiety
- anxiety disorder
- aortic aneurysm
- aortic aneurysm familial thoracic type 3
- aortic aneurysm familial thoracic type 4
- aortic aneurysm familial thoracic type 5
- aortic aneurysm familial thoracic type 6
- aortic arch syndrome
- aortic atheroma
- aortic insufficiency
- aortic sinus aneurysm
- aortic stenosis
- aortic stenosis
- aortic supravalvular stenosis
- aortic valve heart sound a2
- aortic valve replacement
- aortitis
- aortoenteric fistula
- apathy
- Apert-Crouzon syndrome
- aphakia
- aphasia
- aphonia
- aphthous stomatitis
- aplasia cutis congenita with gastrointestinal atresia
- aplastic anemia
- appendicitis
- appetite disorder
- apraxia
- APRT deficiency
- APUDoma
- arachnoid cyst
- arachnoiditis
- arcus senilis
- ARDS
- arenavirus-associated viral hemorrhagic fever syndrome
- argentaffinoma
- arginase deficiency
- argininemia
- argininosuccinate lyase deficiency
- arginosuccinicaciduria
- Argyl-Robertson pupil
- argyria
- argyrophilic grain disease
- Arnold-Chiari malformation
- aromatase deficiency
- aromatase excess syndrome
- aromatic-L-amino-acid decarboxylase deficiency
- arousal
- arrhythmia
- arrhythmia during pregnancy
- arrhythmogenic right ventricular cardiomyopathy
- arrhythmogenic right ventricular cardiomyopathy type 10
- arrhythmogenic right ventricular cardiomyopathy type 11
- arrhythmogenic right ventricular cardiomyopathy type 12
- arrhythmogenic right ventricular cardiomyopathy type 9
- arrhythmogenic right ventricular dysplasia 8
- arsenic poisoning
- arterial dissection
- arterial spider
- arterial thoracic outlet syndrome
- arterial thromboembolism
- arterial thrombosis
- arterial tortuosity syndrome
- arterial ulcer
- arteriohepatic dysplasia
- arteriosclerosis
- arthralgia
- arthritis
- arthritis mutilans
- arthrocutaneouveal granulomatosis
- arthrogryposis multiplex congenita
- arthrogryposis multiplex congenita with pulmonary hypoplasia
- Arthus reaction
- ARTS syndrome
- asbestosis
- Asboe-Hansen sign
- ascending cholangitis
- ascites
- aseptic meningitis
- Asherman's syndrome
- asialism
- aspartylglucosaminuria
- Asperger syndrome
- aspergillosis
- asphyxia
- aspiration pneumonia
- aspiration pneumonitis
- asplenism
- asteatotic dermatitis
- asterixis
- asthenia
- asthenopia
- asthma
- asthma during pregnancy
- asthma in the elderly
- asthma-related traits
- astigmatism
- astroblastoma
- astrocytoma
- astrocytoma grade IV
- asystole
- ataxia
- ataxia telangiectasia
- ataxia telangiectasia like disorder
- ataxia telangiectasia-like disorder
- ataxia, Friedreich-like, with selective vitamin E deficiency
- ataxia-oculomotor apraxia syndrome
- ataxia-telangiectasia variant 1
- ataxic dysarthria
- atelectasis
- atelosteogenesis type II
- Athabascan severe combined immunodeficiency disease
- Athabaskan brainstem dysgenesis syndrome
- atheroembolic renal failure
- atherosclerosis
- atherosclerotic dementia
- athetosis
- athlete's foo
- atonic seizure
- atopic dermatitis
- ATPase synthase deficiency
- atransferrinemia
- atrial arrhythmia
- atrial fibrillation
- atrial fibrillation with bradyarrhythmia
- atrial flutter
- atrial myxoma
- atrial septal aneurysm
- atrial septal defect
- atrial septal defect type 2
- atrial septal defect type 3
- atrial septal defect type 4
- atrial septal defect type 5
- atrial standstill
- atrial tachycardia
- atrichia with papular lesions
- atrioventricular block
- atrioventricular dissociation
- atrioventricular septal defect
- atrophia areata
- atrophic autoimmune thyroiditis
- atrophic vaginitis
- atrophie blanche
- atrophy
- attention disorder
- attention-deficit hyperactivity disorder
- atypical depression
- atypical measles
- atypical meningioma
- atypical seizure
- auditory aphasia
- auditory processing disorder
- aural atresia
- aural polyp
- Auspitz sign
- Austin Flint murmur
- Austin variant of metachromatic leukodystrophy
- autism
- autoimmune disease
- autoimmune epitheliitis
- autoimmune hepatitis
- autoimmune hypophysitis
- autoimmune lymphoproliferative syndrome type 1B
- autoimmune lymphoproliferative syndrome)
- autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy
- autoimmune polyglandular syndrome type 1
- autoimmune polyglandular syndrome type i
- autoimmune thrombocytopenia
- autoimmune thyroid disease
- autologous fat transplantation
- automatism
- autonomic dysfunction
- autosomal dominant adult-onset leukodystrophy
- autosomal dominant aplasia of lacrimal & salivary glands
- autosomal dominant cataracts
- autosomal dominant deafness type 20
- autosomal dominant distal renal tubular acidosis
- autosomal dominant dyskeratosis congenita
- autosomal dominant familial exudative vitreoretinopathy
- autosomal dominant hypercholesterolemia 3
- autosomal dominant hypoparathyroidism
- autosomal dominant keratitis
- autosomal dominant neurosensory deafness 36
- autosomal dominant nonsyndromic deafness 23
- autosomal dominant nonsyndromic sensorineural deafness 14
- autosomal dominant nonsyndromic sensorineural deafness 22
- autosomal dominant nonsyndromic sensorineural deafness 23
- autosomal dominant nonsyndromic sensorineural deafness 28
- autosomal dominant nonsyndromic sensorineural deafness 48
- autosomal dominant osteosclerosis
- autosomal dominant polycystic kidney disease
- autosomal dominant sensorineural deafness 15
- autosomal dominant sensorineural deafness type 10
- autosomal dominant sensorineural deafness type 9
- autosomal liver glycogenosis
- autosomal recessive acute recurrent myoglobinuria
- autosomal recessive congenital cataracts
- autosomal recessive deafness type 10
- autosomal recessive deafness type 2
- autosomal recessive deafness type 31
- autosomal recessive deafness type 8
- autosomal recessive DOPA-responsive dystonia
- autosomal recessive dyskeratosis congenita
- autosomal recessive hypercholesterolemia
- autosomal recessive neurosensory deafness
- autosomal recessive neurosensory deafness 11
- autosomal recessive neurosensory deafness 3
- autosomal recessive neurosensory deafness 4
- autosomal recessive neurosensory deafness 7
- autosomal-dominant dopa-responsive dystonia
- autosplenectomy
- AV junctional rhythm
- AV junctional tachycardia
- AV nodal re-entrant tachycardia
- avascular osteonecrosis
- avian influenza A
- avoidant personality disorder
- Axenfeld-Rieger syndrome
- azoospermia
- azotemia
More General Terms
