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List of diseases starting with A
(Redirected from List of diseases) A listing of diseases.
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Aa-Ab
- Aagenaes syndrome
- Aarskog Ose Pande syndrome
- Aarskog syndrome
- Aase Smith syndrome
- Aase syndrome
- ABCD syndrome
- Abdallat Davis Farrage syndrome
- Abdominal aortic aneurysm
- Abdominal cystic lymphangioma
- Abdominal defects
- Abdominal musculature absent microphthalmia joint laxity
- Abdominal neoplasms
- Aberrant subclavian artery
- Ablepharon macrostomia syndrome
- Ablutophobia
- 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 muscle cramps acral enlargement
- Acarophobia
- 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
- 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
Acr
Acra
- Acral dysostosis dyserythropoiesis
- Acral renal mandibular syndrome
Acro
- Acro coxo mesomelic dysplasia
- Acro fronto facio nasal dysostosis
Acroc-Acrok
- Acrocallosal syndrome, Schinzel type
- Acrocephalopolydactyly
- Acrocephalosyndactyly Jackson Weiss type
- Acrocephaly pulmonary stenosis mental retardation
- Acrodermatitis enteropathica
- Acrodermatitis
- Acrodysostosis
- Acrodysplasia scoliosis
- 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
- Actinomycetales infection
- Activated protein C resistance
Acu
Acut
Acuta
Acute
Acute a-Acute l
Acute m-Acute r
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
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
Ae-Ah
- Aerophobia
- Afibrinogenemia
- Aganglionosis, total intestinal
- Ageing
- Aggressive fibromatosis
- Agnathia holoprosencephaly situs inversus
- Agnosia, primary visual
- Agoraphobia
- Agrizoophobia
- Agyria pachygyria polymicrogyria
- Agyria-pachygyria type 1
- Agyrophobia
- Ahumada-Del Castillo syndrome
Ai-Ak
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 like syndrome
- Albright Turner Morgani syndrome
- Albright's hereditary osteodystrophy
- Albright's syndrome
- Albuminurophobia
- Alcaptonuria
- Alcohol antenatal infection
- Alcohol fetopathy
- Alcoholic hepatitis
- Alcoholic liver cirrhosis
Ald-Alk
All
- Allain Babin Demarquez syndrome
- Allan Herndon syndrome
- Allanson Pantzar McLeod syndrome
- Allergic angiitis
- Allergic autoimmune thyroiditis
- Allergic bronchopulmonary aspergillosis
- Allergic encephalomyelitis
- Alliumphobia
- Allodoxaphobia
Alo
- Aloi Tomasini Isaia syndrome
- 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
- Alopecia
Alp-Alz
Am
Ama-Ame
- Amathophobia
- Amaurosis congenita of Leber, type 1
- Amaurosis congenita of Leber, type 2
- Amaurosis congenita of Leber
- Amaurosis hypertrichosis
- Amaxophobia
- Amblyopia
- Ambral syndrome
- Ambras syndrome
- Ambulophobia
- Amegakaryocytic thrombocytopenia
- Amelia cleft lip palate hydrocephalus iris coloboma
- Amelia facial dysmorphism
- Amelia X linked
- Amelogenesis Imperfecta hypomaturation type
- Amelogenesis imperfecta local hypoplastic form
- Amelogenesis imperfecta nephrocalcinosis
- Amelogenesis imperfecta
- Ameloonychohypohidrotic syndrome
- Amenorrhea, Primary
- American trypanosomiasis
Ami-Amy
- Aminoacidopathies
- Aminoaciduria
- Aminopterin antenatal infection
- Aminopterin like syndrome without aminopterin
- Amniotic bands
- Amoebiasis due to Entamoeba histolytica
- Amoebiasis due to free-living amoebae
- Amoebiasis or Amebiasis
- Ampola syndrome
- Amychophobia
- Amylo-1,6-glucosidase deficiency
- Amyloid angiopathy
- Amyloid Neuropathies, Familial
- Amyloid polyneuropathy, transthyretin related
- Amyloidosis of gingiva and conjunctiva mental retardation
- Amyloidosis, Familial
- Amyloidosis
- Amylopectinosis
- Amyoplasia mandibulofacial dysostosis
- Amyoplasia
- Amyotonia congenita
- Amyotrophic lateral sclerosis
An
Ana-Ane
Ang
- Angel shaped phalangoepiphyseal dysplasia
- Angelman syndrome
- Angiofollicular ganglionic hyperplasia
- Angiofollicular lymph hyperplasia
- Angioimmunoblastic with dysproteinemia lymphadenopathy
- Angiokeratoma mental retardation coarse face
- Angiolipoma
- Angioma hereditary neurocutaneous
- Angiomatosis encephalotrigeminal
- Angiomatosis leptomeningeal capillary - venous
- Angiomatosis systemic cystic Seip syndrome
- Angiomyomatous Hamartoma
- Angioneurotic edema hereditary due to C1 esterase deficiency
- 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 of teeth
- Ankylostomiasis
Ann
- Annular constricting bands
- Annular pancreas
- Annuloaortic ectasia
Ano
- Anodontia
- Anonychia ectrodactyly
- Anonychia microcephaly
- Anonychia onychodystrophy brachydactyly type B
- Anonychia onychodystrophy
- Anophthalia pulmonary hypoplasia
- 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 with limb anomalies
- Anophthalmos, clinical
- Anorchia
- Anorchidism
- Anorectal anomalies
- Ano-rectal atresia
- Anorexia nervosa
- Anosmia
- Anotia facial palsy cardiac defect
- Anotia
Ans-Ant
Ao
Ap
Ape-App
- Apert like polydactyly syndrome
- Apert syndrome
- Aphalangia hemivertebrae
- Aphalangia syndactyly microcephaly
- Aphthous stomatitis
- Apiphobia
- 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
- Apo A-I deficiency
- Apolipoprotein C-II deficiency
- Apparent mineralocorticoid excess
- Appendicitis
Apr-Apu
- Apraxia manual
- Apraxia, Ideomotor
- Apraxia, ocular motor, Cogan type
- Apraxia
- Apudoma
Aq
- Aqueductal stenosis, X linked
Ar
Ara-Aro
- Arachindonic acid, absence of
- Arachnodactyly ataxia cataract aminoaciduria mental retardation
- Arachnodactyly mental retardation dysmorphism
- Arachnoid cysts
- Arachnoiditis
- Arakawa'sa syndrome II
- Arbovirosis
- Arc syndrome
- Aredyld syndrome
- AREDYLD
- Arginase deficiency
- Arginemia
- Argininosuccinate synthetase deficiency
- Argininosuccinic aciduria
- Argyria
- Arhinia choanal atresia microphthalmia
- Arnold Stckler Bourne syndrome
- Arnold-Chiari malformation
- Arnold-Chiari syndrome
- Aromatase deficiency
- Aromatic amino acid decarboxylase deficiency
Arr
Art
Arte
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
- Arylsulfatase A deficiency
As
At
Au-Az
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