Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/1
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- Abdominal musculature absent microphthalmia joint laxity
- Abdominal neoplasms
- Ablepharon macrostomia syndrome
- Abnormal systemic venous return
- Absence of tibia with polydactyly
- Absent corpus callosum cataract immunodeficiency
- Acanthocytosis chorea
- Acanthosis nigricans muscle cramps acral enlargement
- Accessory deep peroneal nerve
- Achalasia alacrimia syndrome
- Achalasia microcephaly
- Achalasia, familial esophageal
- Achalasia-Addisonianism-Alacrimia syndrome
- Achondrogenesis Kozlowski type
- Achondroplasia Swiss type agammaglobulinemia
- Achromatopsia incomplete, X-linked
- Acitretine antenatal infection
- Acquired agranulocytosis
- Acquired hypoprothrombinemia
- Acquired prothrombin deficiency
- Acral dysostosis dyserythropoiesis
- Acral renal mandibular syndrome
- Acro coxo mesomelic dysplasia
- Acro fronto facio nasal dysostosis
- Acrocallosal syndrome, Schinzel type
- Acrocephalopolydactyly
- Acrocephalosyndactyly Jackson Weiss type
- Acrocephaly pulmonary stenosis mental retardation
- 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, Palagonia type
- Acrokeratoelastoidosis of Costa
- Acromegaloid changes cutis verticis gyrata corneal
- Acromegaloid facial appearance syndrome
- Acromegaloid hypertrichosis syndrome
- Acromesomelic dysplasia Brahimi Bacha type
- Acromesomelic dysplasia Campailla Martinelli type
- Acromesomelic dysplasia Hunter Thompson type
- Acromesomelic dysplasia, Maroteaux type
- Acromesomelic dysplasia
- Acroosteolysis dominant type
- Acroosteolysis neurogenic
- Acroosteolysis osteoporosis skull and mandible changes
- Acropectoral syndrome
- Acropectorenal field defect
- Acropectorovertebral dysplasia
- Acropigmentation of Dohi
- Acrorenal syndrome recessive
- Acrorenoocular syndrome
- Acute articular rheumatism
- Acute idiopathic polyneuritis
- Acute lymphoblastic leukemia congenital sporadic aniridia
- Acute megakaryoblastic leukemia
- Acute monoblastic leukemia
- Acute myeloblastic leukemia with maturation
- Acute myeloblastic leukemia without maturation
- Acute myelomonocytic leukemia
- Acute posterior multifocal placoid pigment epitheliopathy
- Acyl-CoA oxidase deficiency
- Adactylia unilateral dominant
- Adam complex familial
- Adducted thumb club foot syndrome
- Adducted thumbs Dundar type
- Adenocarcinoid tumor
- Adenomelablastoma
- Adenosine triphosphatase deficiency, anemia due to
- Adolescent benign focal crisis
- Adrenal adenoma, familial
- Adrenal disorder
- Adrenal gland hyperfunction
- Adrenal gland hypofunction
- Adrenal hypertension
- Adrenal hypoplasia congenital, X-linked
- Adrenal hypoplasia
- Adrenal macropolyadenomatosis
- Adrenal medulla neoplasm
- Adrenomyodystrophy
- Adult spinal muscular atrophy
- Adult syndrome
- Aganglionosis, total intestinal
- Aggressive fibromatosis
- Agnathia holoprosencephaly situs inversus
- Agnosia, primary visual
- Agyria pachygyria polymicrogyria
- Agyria-pachygyria type 1
- Ahumada-Del Castillo syndrome
- Aicardi-Goutieres syndrome
- AIDS dysmorphic syndrome
- Akaba Hayasaka syndrome
- Akesson syndrome
- Aksu Stckhausen syndrome
- 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
- Alar nasal cartilages coloboma of telecanthus
- Albers-Schonberg disease
- Albinism deafness syndrome
- Albinism ocular late onset sensorineural deafness
- Albinism oculocutaneous, Hermansky-Pudlak type
- Albinism, minimal pigment type
- Albinism, yellow mutant type
- Albrecht Schneider Belmont syndrome
- Albright like syndrome
- Albright Turner Morgani syndrome
- Alcohol antenatal infection
- Aldolase A deficiency
- Aldred syndrome
- Aleukemic leukemia cutis
- Allain Babin Demarquez syndrome
- Allan Herndon syndrome
- Allanson Pantzar McLeod syndrome
- Allergic autoimmune thyroiditis
- Allergic encephalomyelitis
- Aloi Tomasini Isaia syndrome
- Alopecia anosmia deafness hypogonadism syndrome
- 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 universalis onychodystrophy vitiligo
- Alopecia, epilepsy, pyorrhea, mental subnormality
- Alpha-2 deficient collagen disease
- Alpha-ketoglutarate dehydrogenase deficiency
- Alpha-L-iduronidase deficiency
- Alpha-sarcoglycanopathy
- Alpha-thalassemia-abnormal morphogenesis
- Alport syndrome macrothrombocytopenia
- Alport syndrome, dominant type
- Alport syndrome, recessive type
- Aluminium lung
- Alveolar echinococcosis
- Alves Dos Santos Castello syndrome
- Amaurosis congenita of Leber, type 1
- Amaurosis congenita of Leber, type 2
- Amaurosis congenita of Leber
- Amaurosis hypertrichosis
- Ambral syndrome
- 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
- Ameloonychohypohidrotic syndrome
- Aminoacidopathies
- Aminopterin antenatal infection
- Aminopterin like syndrome without aminopterin
- Amoebiasis due to Entamoeba histolytica
- Amoebiasis due to free-living amoebae
- Ampola syndrome
- Amylo-1,6-glucosidase deficiency
- Amyloid angiopathy
- Amyloid Neuropathies, Familial
- Amyloid polyneuropathy, transthyretin related
- Amyloidosis of gingiva and conjunctiva mental retardation
- Amyloidosis, Familial
- Amylopectinosis
- Amyoplasia mandibulofacial dysostosis
- Amyotonia congenita
- Anablephobia
- Andersen's disease
- Andre syndrome
- Anemia sideroblastic spinocerebellar ataxia
- Anemia, Hypoplastic, Congenital
- Anencephaly spina bifida X linked
- Aneurysm, intracranial berry
- Angel shaped phalangoepiphyseal dysplasia
- Angiofollicular ganglionic hyperplasia
- Angiofollicular lymph hyperplasia
- Angioimmunoblastic lymphadenopathy with dysproteinemia
- 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
- 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
- Ankle defects short stature
- Ankyloblepharon ectodermal defects cleft lip palate
- Ankyloblepharon filiforme adnatum cleft palate
- Ankyloblepharon filiforme imperforate anus
- Ankyloglossia heterochromia clasped thumbs
- Ankylosing vertebral hyperostosis with tylosis
- Ankylosis of teeth
- Annular constricting bands
- Annuloaortic ectasia
- 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
- Anorectal anomalies
- Ano-rectal atresia
- Anotia facial palsy cardiac defect
- Ansell Bywaters Elderking syndrome
- Anterior pituitary insufficiency, familial
- Anti-factor VIII autoimmunization
- Antigen-peptide-transporter 2 deficiency
- Anti-HLA hyperimmunization
- Antihypertensive drugs antenatal infection
- Antinolo Nieto Borrego syndrome
- Anti-plasmin deficiency, congenital
- Antisynthetase syndrome
- Antley-Bixler syndrome
- Aorta-pulmonary artery fistula
- Aortic arch anomaly peculiar facies mental retardation
- Aortic arches defect
- Aortic dissection lentiginosis
- Aortic supravalvular stenosis
- Aortic valves stenosis of the child
- Aortic window
- Apert like polydactyly syndrome
- Aphalangia hemivertebrae
- Aphalangia syndactyly microcephaly
- 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
- Apo A-I deficiency
- Apolipoprotein C-II deficiency
- Apraxia manual
- Apraxia, Ideomotor
- Apraxia, ocular motor, Cogan type
- Apudoma
- Aqueductal stenosis, X linked
- Arachindonic acid, absence of
- Arachnodactyly ataxia cataract aminoaciduria mental retardation
- Arachnodactyly mental retardation dysmorphism
- Arbovirosis
- Arc syndrome
- Aredyld syndrome
- Arhinia choanal atresia microphthalmia
- Arnold Stckler Bourne syndrome
- Aromatase deficiency
- Aromatic amino acid decarboxylase deficiency
- Arroyo Garcia Cimadevilla syndrome
- Arrythmogenic right ventricular dysplasia, familial
- Arterial calcification of infancy
- Arterial dysplasia
- Arterial tortuosity
- Arthritis short stature deafness
- 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 ophthalmoplegia retinopathy
- Arthrogryposis renal dysfunction cholestasis syndrome
- Arthrogryposis spinal muscular atrophy
- Arylsulfatase A deficiency
- Ascher's Syndrome
- Asymmetric septal hypertrophy
- Ataxia telangiectasia variant V1
- Ataxia, Marie's
- Athabaskan brain stem dysgenesis
- Atresia of small intestine
- Atrial myxoma, familial
- Atrophoderma of Pierini and Pasini
- Attenuated FAP
- Atypical lipodystrophy
- Auditory Perceptual Disorder
- Aughton syndrome
- Ausems Wittebol Post Hennekam syndrome
- Autoimmune peripheral neuropathy
- Axial mesodermal dysplasia spectrum
- Axial osteomalacia
- Axial osteosclerosis
