List of diseases (A)
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Diseases |
Aa-Ab
- Aagenaes syndrome
- Aarskog Ose Pande syndrome
- Aarskog syndrome
- Aase Smith syndrome
- Aase syndrome
- ABCD syndrome
- Abasia
- Abdallat Davis Farrage syndrome
- Abdominal aortic aneurysm
- Abdominal cystic lymphangioma
- Abdominal defects
- Abdominal musculature absent microphthalmia joint laxity
- Abdominal neoplasm / Abdominal neoplasms
- Aberrant subclavian artery
- Ablepharon macrostomia syndrome
- Abnormal systemic venous return
- Abruzzo Erickson syndrome
- Absence of Gluteal muscle
- Absence of tibia with polydactyly
- Absent corpus callosum cataract immunodeficiency
- Absent T lymphocytes
Ac
Aca-Acc
- Acalvaria
- Acanthocheilonemiasis
- Acanthocytosis chorea
- Acanthocytosis
- Acanthosis nigricans
- Acatalasemia
- Accessory deep peroneal nerve
- Accessory Navicular bone
- Accessory pancreas
Ach-Ack
- Achalasia alacrimia syndrome
- Achalasia microcephaly
- Achalasia, familial esophageal
- Achalasia
- Achalasia-Addisonianism-Alacrimia syndrome
- Achard syndrome
- Achard-Thiers syndrome
- Acheiropodia
- Achondrogenesis Kozlowski type
- Achondrogenesis type 1A
- Achondrogenesis type 1B
- Achondrogenesis type 2
- Achondrogenesis
- Achondroplasia Swiss type agammaglobulinemia
- Achondroplasia
- Achondroplastic dwarfism
- Achromatopsia incomplete, X-linked
- Achromatopsia
- Acid maltase deficiency
- Acidemia, isovaleric
- Acidemia, propionic
- Acitretine antenatal infection
- Ackerman syndrome
Acn-Acq
- Acne rosacea
- Acne
- Acoustic neuroma
- Acoustic schwannomas
- Acquired agranulocytosis
- Acquired hypoprothrombinemia
- Acquired Immune Deficiency Syndrome
- Acquired ichthyosis
- Acquired prothrombin deficiency
- Acquired syphilis
Acr
Acra
Acro
Acroc-Acrok
- Acrocallosal syndrome, Schinzel type
- Acrocephalopolydactyly
- Acrocephalosyndactyly Jackson Weiss type
- Acrocephaly
- Acrocephaly pulmonary stenosis mental retardation
- Acrocyanosis
- Acrodermatitis enteropathica
- Acrodermatitis
- Acrodysostosis
- Acrodysplasia
- Acrodysplasia scoliosis
- Acrofacial dysostosis
- Acrofacial dysostosis ambiguous genitalia
- Acrofacial dysostosis atypical postaxial
- Acrofacial dysostosis Catania form
- Acrofacial dysostosis Preis type
- Acrofacial dysostosis Rodriguez type
- Acrofacial dysostosis Weyers type
- Acrofacial dysostosis, Nager type
- Acrofacial dysostosis, Palagonia type
- Acrokeratoelastoidosis of Costa
Acrom-Acros
- Acromegaloid changes cutis verticis gyrata corneal
- Acromegaloid facial appearance syndrome
- Acromegaloid hypertrichosis syndrome
- Acromegaly
- Acromesomelic dysplasia Brahimi Bacha type
- Acromesomelic dysplasia Campailla Martinelli type
- Acromesomelic dysplasia Hunter Thompson type
- Acromesomelic dysplasia, Maroteaux type
- Acromesomelic dysplasia
- Acromicric dysplasia
- Acroosteolysis dominant type
- Acroosteolysis neurogenic
- Acroosteolysis osteoporosis skull and mandible changes
- Acropectoral syndrome
- Acropectorenal field defect
- Acropectorovertebral dysplasia
- Acrophobia
- Acropigmentation of Dohi
- Acrorenal syndrome recessive
- Acrorenoocular syndrome
- Acrospiroma
Act
- ACTH deficiency
- ACTH resistance
- Atelectasis
- Actinic keratosis
- Actinomycetales infection
- Actinomycosis
- Activated protein C resistance
Acu
Acut
Acuta
Acute
Acute a-Acute l
- Acute articular rheumatism
- Acute erythroblastic leukemia
- Acute febrile neutrophilic dermatosis
- Acute gouty arthritis
- Acute idiopathic polyneuritis
- Acute intermittent porphyria
- Acute lymphoblastic leukemia congenital sporadic aniridia
- Acute lymphoblastic leukemia
- Acute lymphocytic leukemia
Acute m-Acute p
- Acute megakaryoblastic leukemia
- Acute monoblastic leukemia
- Acute monocytic leukemia
- Acute mountain sickness
- Acute myeloblastic leukemia type 1
- Acute myeloblastic leukemia type 2
- Acute myeloblastic leukemia type 3
- Acute myeloblastic leukemia type 4
- Acute myeloblastic leukemia type 5
- Acute myeloblastic leukemia type 6
- Acute myeloblastic leukemia type 7
- Acute myeloblastic leukemia with maturation
- Acute myeloblastic leukemia without maturation
- Acute myelocytic leukemia
- Acute myelogenous leukemia
- Acute myeloid leukemia (generic term)
- Acute myeloid leukemia, secondary
- Acute myelomonocytic leukemia
- Acute necrotizing ulcerative gingivitis
- Acute non lymphoblastic leukemia (generic term)
- Acute pancreatitis
- Acute posterior multifocal placoid pigment epitheliopathy
- Acute promyelocytic leukemia
Acute r-Acute t
Acy
- Acyl-CoA dehydrogenase, medium chain, deficiency of
- Acyl-CoA dehydrogenase, short chain, deficiency of
- Acyl-CoA dehydrogenase, very long chain, deficiency of
- Acyl-CoA oxidase deficiency
Ad
Ada-Adi
- Adactylia unilateral dominant
- Adam complex familial
- Adams Nance syndrome
- Adams-Oliver syndrome
- Addiction
- Addison's disease
- Adducted thumb club foot syndrome
- Adducted thumb syndrome recessive form
- Adducted thumbs Dundar type
- Adenine phosphoribosyltransferase deficiency
- Adenocarcinoid tumor
- Adenocarcinoma of lung
- Adenoid cystic carcinoma
- Adenoma of the adrenal gland
- Adenoma
- Adenomelablastoma
- Adenomyosis
- Adenosine deaminase deficiency
- Adenosine monophosphate deaminase deficiency
- Adenosine triphosphatase deficiency, anemia due to
- Adenylosuccinate lyase deficiency
- Adie syndrome
- Adiposis dolorosa aka Dercum's disease
Ado-Adr
- Adolescent benign focal crisis
- Adrenal adenoma, familial
- Adrenal cancer
- Adrenal disorder
- Adrenal gland hyperfunction
- Adrenal gland hypofunction
- Adrenal hyperplasia, congenital
- Adrenal hyperplasia
- Adrenal hypertension
- Adrenal hypoplasia congenital, X-linked
- Adrenal hypoplasia
- Adrenal incidentaloma
- Adrenal insufficiency
- Adrenal macropolyadenomatosis
- Adrenal medulla neoplasm
- Adrenocortical carcinoma
- Adrenogenital syndrome
- Adrenoleukodystrophy, autosomal, neonatal form
- Adrenoleukodystrophy, X-linked
- Adrenoleukodystrophy
- Adrenomyodystrophy
Adu
- Adult onset Still's disease
- Adult spinal muscular atrophy
- Adult syndrome
- Advanced sleep phase syndrome
Ae-Ah
- Afibrinogenemia
- Agammaglobulinemia
- Aganglionosis
- Aganglionosis, total intestinal
- Aging
- Aggressive fibromatosis
- Agnathia
- Agnathia holoprosencephaly situs inversus
- Agnosia, primary visual
- Agoraphobia
- Agyria
- Agyria pachygyria polymicrogyria
- Agyria-pachygyria type 1
- Ahumada-Del Castillo syndrome
Ai-Ak
- Aicardi syndrome
- Aicardi-Goutières syndrome
- Aichmophobia
- AIDS
- AIDS Dementia Complex
- AIDS dysmorphic syndrome
- Ainhum
- Akaba Hayasaka syndrome
- Akesson syndrome
- Aksu Stckhausen syndrome
Al
- Al Awadi Teebi Farag syndrome
- Al Frayh Facharzt Haque syndrome
- Al Gazali Al Talabani syndrome
- Al Gazali Aziz Salem syndrome
- Al Gazali Donnai Mueller syndrome
- Al Gazali Hirschsprung syndrome
- Al Gazali Khidr Prem Chandran syndrome
- Al Gazali Sabrinathan Nair syndrome
Ala-Alc
- Alagille-Watson syndrome (AWS)
- Alar nasal cartilages coloboma of telecanthus
- Albers-Schonberg disease
- Albinism deafness syndrome
- Albinism immunodeficiency
- Albinism ocular late onset sensorineural deafness
- Albinism oculocutaneous, Hermansky-Pudlak type
- Albinism, minimal pigment type
- Albinism, ocular
- Albinism, yellow mutant type
- Albinism
- Albinoidism
- Albrecht Schneider Belmont syndrome
- Albright Turner Morgani syndrome
- Albright's hereditary osteodystrophy
- Albright's syndrome
- Alcaptonuria
- Alcohol antenatal infection
- Alcohol fetopathy
- Alcoholic hepatitis
- Alcoholic liver cirrhosis
Ald-All
- Aldolase A deficiency
- Aldred syndrome
- Aleukemic leukemia cutis
- Alexander disease
- Alien hand syndrome
- Alkaptonuria
- Allain Babin Demarquez syndrome
- Allan Herndon syndrome
- Allanson Pantzar McLeod syndrome
- Allergic angiitis
- Allergic autoimmune thyroiditis
- Allergic bronchopulmonary aspergillosis
- Allergic encephalomyelitis
Alo
- Aloi Tomasini Isaia syndrome
- Alopecia
- Alopecia anosmia deafness hypogonadism syndrome
- Alopecia areata
- Alopecia congenita keratosis palmoplantaris
- Alopecia contractures dwarfism mental retardation
- Alopecia epilepsy oligophrenia syndrome of Moynahan
- Alopecia hypogonadism extrapyramidal disorder
- Alopecia immunodeficiency
- Alopecia macular degeneration growth retardation
- Alopecia mental retardation hypogonadism
- Alopecia mental retardation syndrome
- Alopecia totalis
- Alopecia universalis onychodystrophy vitiligo
- Alopecia universalis
- Alopecia, epilepsy, pyorrhea, mental subnormality
Alp-Alz
- Alpers disease
- Alpha 1-antitrypsin deficiency
- Alpha-2 deficient collagen disease
- Alpha-ketoglutarate dehydrogenase deficiency
- Alpha-L-iduronidase deficiency
- Alpha-mannosidosis
- Alpha-sarcoglycanopathy
- Alpha-thalassemia
- Alpha-thalassemia-abnormal morphogenesis
- Alport syndrome macrothrombocytopenia
- Alport syndrome, dominant type
- Alport syndrome, recessive type
- Alport syndrome
- Alstrom's syndrome
- Alternating hemiplegia of childhood
- Alternating hemiplegia
- Aluminium lung
- Alveolar Capillary Dysplasia
- Alveolar echinococcosis
- Alveolar soft part sarcoma
- Alveolitis, extrinsic allergic
- Alves Dos Santos Castello syndrome
- Alzheimer's disease
- Alzheimer disease, familial
Am
Ama-Ame
- Amaurosis
- Amaurosis congenita of Leber, type 1
- Amaurosis congenita of Leber, type 2
- Amaurosis congenita of Leber
- Amaurosis hypertrichosis
- Amblyopia
- Ambral syndrome
- Ambras syndrome
- Amegakaryocytic thrombocytopenia
- Amelia (birth defect)
- Amelia cleft lip palate hydrocephalus iris coloboma
- Amelia facial dysmorphism
- Amelia X linked
- Amelogenesis
- Amelogenesis Imperfecta hypomaturation type
- Amelogenesis imperfecta local hypoplastic form
- Amelogenesis imperfecta nephrocalcinosis
- Amelogenesis imperfecta
- Ameloonychohypohidrotic syndrome
- Amenorrhea
- American trypanosomiasis
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An
Ana-Ane
- Anaphylaxis
- Anaplastic thyroid cancer
- Andersen's disease
- Andre syndrome
- Androgen insensitivity syndrome (AIS)
- Anemia sideroblastic spinocerebellar ataxia
- Anemia, Diamond-Blackfan
- Anemia, Hypoplastic, Congenital
- Anemia, Pernicious
- Anemia, Sideroblastic
- Anemia
- Anencephaly spina bifida X linked
- Anencephaly
- Aneurysm of sinus of Valsalva
- Aneurysm, intracranial berry
- Aneurysm
Ang
- Angel shaped phalangoep
- Angiofollicular lymph hyperplasia
- Angioimmunoblastic lymphadenopathy with dysproteinemia
- Angiokeratoma mental retardation coarse face
- Angiolipoma
- Angioma
- Angioma hereditary neurocutaneous
- Angiomatosis
- Angiomatosis encephalotrigeminal
- Angiomatosis leptomeningeal capillary - venous
- Angiomatosis systemic cystic seip syndrome
- Angiomyomatous hamartoma
- Angioneurotic edema hereditary due to C1 esterase deficiency
- Angiosarcoma
- Angiosarcoma of the liver
- Angiosarcoma of the scalp
- Angiostrongyliasis
- Angiotensin renin aldosterone hypertension
- Anguillulosis
Ani-Ank
- Aniridia absent patella
- Aniridia ataxia renal agenesis psychomotor retardation
- Aniridia cerebellar ataxia mental deficiency
- Aniridia mental retardation syndrome
- Aniridia ptosis mental retardation obesity familial
- Aniridia renal agenesis psychomotor retardation
- Aniridia type 2
- Aniridia, sporadic
- Aniridia
- Anisakiasis
- Ankle defects short stature
- Ankyloblepharon ectodermal defects cleft lip palate
- Ankyloblepharon filiforme adnatum cleft palate
- Ankyloblepharon filiforme imperforate anus
- Ankyloglossia heterochromia clasped thumbs
- Ankylosing spondylarthritis
- Ankylosing spondylitis
- Ankylosing vertebral hyperostosis with tylosis
- Ankylosis
- Ankylosis of teeth
- Ankylostomiasis
Ann
Ano
- Anodontia
- Anonychia
- Anonychia ectrodactyly
- Anonychia microcephaly
- Anonychia onychodystrophy brachydactyly type B
- Anonychia onychodystrophy
- Anophthalia
- Anophthalia pulmonary hypoplasia
- Anophthalmia
- Anophthalmia cleft lip palate hypothalamic disorder
- Anophthalmia cleft palate micrognathia
- Anophthalmia esophageal atresia cryptorchidism
- Anophthalmia megalocornea cardiopathy skeletal anomalies
- Anophthalmia microcephaly hypogonadism
- Anophthalmia plus syndrome
- Anophthalmia short stature obesity
- Anophthalmia Waardenburg syndrome
- Anophthalmos
- Anophthalmos with limb anomalies
- Anophthalmos, clinical
- Anorchia
- Anorchidism
- Anorectal anomalies
- Anorectal atresia / Ano-rectal atresia
- Anorexia nervosa
- Anosmia
- Anotia facial palsy cardiac defect
- Anotia
Ans-Ant
- Ansell Bywaters Elderking syndrome
- Anterior horn disease
- Anterior pituitary insufficiency, familial
- Anthrax
- Anti-factor VIII autoimmunization
- Antigen-peptide-transporter 2 deficiency
- Anti-HLA hyperimmunization
- Antihypertensive drugs antenatal infection
- Antinolo Nieto Borrego syndrome
- Antiphospholipid syndrome
- Anti-plasmin deficiency
- Anti-plasmin deficiency, congenital
- Antisocial personality disorder
- Antisynthetase syndrome
- Antithrombin deficiency, congenital
- Antley-Bixler syndrome
- Anton syndrome
Ao
- Aorta-pulmonary artery fistula
- Aortic aneurysm
- Aortic arch anomaly peculiar facies mental retardation
- Aortic arch interruption
- Aortic arches defect
- Aortic coarctation
- Aortic dissection
- Aortic dissection lentiginosis
- Aortic supravalvular stenosis
- Aortic valve stenosis
- Aortic valves stenosis of the child
- Aortic window
Ap
Ape-App
- Apert like polydactyly syndrome
- Apert syndrome
- Aphalangia
- Aphalangia hemivertebrae
- Aphalangia syndactyly microcephaly
- Aphthous stomatitis
- Apiphobia
- Aplasia
- Aplasia cutis autosomal recessive
- Aplasia cutis congenita dominant
- Aplasia cutis congenita epibulbar dermoids
- Aplasia cutis congenita intestinal lymphangiectasia
- Aplasia cutis congenita of limbs recessive
- Aplasia cutis congenita recessive
- Aplasia cutis congenita
- Aplasia cutis myopia
- Aplasia/hypoplasia of pelvis, femur, fibula, and ulna with abnormal digits and nails
- Aplastic anemia
- Aplastic crisis
- Apo A-I deficiency
- Apolipoprotein C-II deficiency
- Apparent mineralocorticoid excess
- Appelt-Gerken-Lenz syndrome
- Appendicitis
Apr-Apu
Aq
Ar
Ara-Aro
- Arachindonic acid, absence of
- Arachnodactyly
- Arachnodactyly ataxia cataract aminoaciduria mental retardation
- Arachnodactyly mental retardation dysmorphism
- Arachnoid cysts
- Arachnoiditis
- Arakawa's syndrome II
- Arbovirosis
- Arc syndrome
- Aredyld syndrome
- AREDYLD
- Arginase deficiency
- Arginemia
- Argininosuccinate synthetase deficiency
- Argininosuccinic aciduria
- Argyria
- Arhinia
- Arhinia choanal atresia microphthalmia
- Arnold Stickler Bourne syndrome
- Arnold-Chiari malformation
- Aromatase deficiency
- Aromatic amino acid decarboxylase deficiency
Arr
- Arrhinia
- Arrhythmogenic right ventricular dysplasia
- Arroyo Garcia Cimadevilla syndrome
- Arrythmogenic right ventricular dysplasia, familial
Art
Arte
- Arterial calcification of infancy
- Arterial dysplasia
- Arterial tortuosity
- Arteriovenous malformation
- Arteritis
Arth
- Arthritis short stature deafness
- Arthritis, Juvenile
- Arthritis
- Arthrogryposis due to muscular dystrophy
- Arthrogryposis ectodermal dysplasia other anomalies
- Arthrogryposis epileptic seizures migrational brain disorder
- Arthrogryposis IUGR thoracic dystrophy
- Arthrogryposis like disorder
- Arthrogryposis like hand anomaly sensorineural
- Arthrogryposis multiplex congenita CNS calcification
- Arthrogryposis multiplex congenita distal
- Arthrogryposis multiplex congenita neurogenic type
- Arthrogryposis multiplex congenita pulmonary hypoplasia
- Arthrogryposis multiplex congenita whistling face
- Arthrogryposis multiplex congenita, distal type 1
- Arthrogryposis multiplex congenita, distal type 2
- Arthrogryposis multiplex congenita, distal, x-linked
- Arthrogryposis multiplex congenita
- Arthrogryposis ophthalmoplegia retinopathy
- Arthrogryposis renal dysfunction cholestasis syndrome
- Arthrogryposis spinal muscular atrophy
- Arthrogryposis
Ary
As
- Asbestosis
- Ascariasis
- Ascher's syndrome
- Aseptic meningitis
- Asherman's syndrome
- Ashman's phenomenon
- Aspartylglycosaminuria
- Aspergillosis
- Asphyxia neonatorum
- Aspiration pneumonia
- Asplenia
- Astasis
- Astasia-abasia
- Asthenia
- Asthma
- Astrocytoma
- Asymmetric septal hypertrophy
At
- Ataxia
- Ataxia telangiectasia variant V1
- Ataxia telangiectasia
- Ataxia, Marie's
- Atelectasis
- Atelosteogenesis, type II
- Athabaskan brain stem dysgenesis
- Atherosclerosis
- Athetosis
- Athlete's foot
- Atopic Dermatitis
- Atresia
- Atresia of small intestine
- Atrial myxoma
- Atrial septal defect
- Atrioventricular fistula
- Atrioventricular septal defect
- Atrophic vaginitis
- Atrophoderma
- Atrophoderma of Pierini and Pasini
- Atrophy
- ATR-X
- Attention Deficit Hyperactivity Disorder
- Attenuated FAP
- Atypical lipodystrophy
Au-Az
- Aughton syndrome
- Ausems Wittebol Post Hennekam syndrome
- Autoimmune hemolytic anemia
- Autoimmune hepatitis
- Autoimmune peripheral neuropathy
- Autoimmune polyendocrinopathy syndrome, type I
- Autonomic dysfunction
- Autonomic nervous system diseases
- Axial mesodermal dysplasia
- Axial mesodermal dysplasia spectrum
- Axial osteomalacia
- Axial osteosclerosis
- Ayazi syndrome
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
