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5 Oxoprolinuria   |   Aagenaes syndrome   |   Aarskog Ose Pande syndrome   |   Aarskog Syndrome   |   Aase Smith syndrome   |   Aase Syndrome   |   ABCD syndrome   |   Abdallat Davis Farage syndrome   |   Abdominal aortic aneurysm   |   Abdominal cystic lymphangioma   |   Abdominal defects   |   Abdominal musculature absent microphthalmia joint laxity   |   Abdominal neoplasms   |   Aberrant subclavian artery   |   Abetalipoproteinemia   |   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   |   Acalvaria   |   Acanthocheilonemiasis   |   Acanthocytosis   |   Acanthocytosis chorea   |   Acanthosis Nigricans   |   Acanthosis nigricans muscle cramps acral enlargement   |   Acarophobia   |   Acatalasemia   |   Accessory deep peroneal nerve   |   Accessory Navicular bone   |   Accessory pancreas   |   Achalasia   |   Achalasia alacrimia syndrome   |   Achalasia microcephaly   |   Achalasia, familial esophageal   |   Achalasia-Addisonianism-Alacrimia syndrome   |   Achard syndrome   |   Achard Thiers Syndrome   |   Achard-Thiers syndrome   |   Acheiropodia   |   Achondrogenesis   |   Achondrogenesis Kozlowski type   |   Achondrogenesis type 1A   |   Achondrogenesis type 1B   |   Achondroplasia   |   Achondroplasia Swiss type agammaglobulinemia   |   Achondroplastic dwarfism   |   Achromatopsia   |   Achromatopsia incomplete, X-linked   |   Acid maltase deficiency   |   Acidemia, Isovaleric   |   Acidemia, Methylmalonic   |   Acidemia, Propionic   |   Acitretine antenatal infection   |   Ackerman syndrome   |   Acne   |   Acne Rosacea   |   Acoustic Neuroma   |   Acoustic schwannomas   |   Acquired agranulocytosis   |   Acquired Aplastic Anemia   |   Acquired hypoprothrombinemia   |   Acquired ichthyosis   |   Acquired Immune Deficiency Syndrome   |   Acquired prothrombin deficiency   |   Acquired syphilis   |   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   |   Acrodermatitis Enteropathica   |   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   |   Acromegaloid changes cutis verticis gyrata corneal   |   Acromegaloid facial appearance syndrome   |   Acromegaloid hypertrichosis syndrome   |   Acromegaly   |   Acromesomelic Dysplasia   |   Acromesomelic dysplasia Brahimi Bacha type   |   Acromesomelic dysplasia Campailla Martinelli type   |   Acromesomelic dysplasia Hunter Thompson type   |   Acromesomelic dysplasia, Maroteaux type   |   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   |   ACTH Deficiency   |   ACTH resistance   |   Actinomycetales infection   |   Actinomycosis   |   Activated protein C resistance   |   Acutane embryopathy   |   Acute articular rheumatism   |   Acute erythroblastic leukemia   |   Acute febrile neutrophilic dermatosis   |   Acute idiopathic polyneuritis   |   Acute intermittent porphyria   |   Acute lymphoblastic leukemia   |   Acute lymphoblastic leukemia congenital sporadic aniridia   |   Acute lymphocytic leukemia   |   Acute megakaryoblastic leukemia   |   Acute monoblastic 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 posterior multifocal placoid pigment epitheliopathy   |   Acute promyelocytic leukemia   |   Acute renal failure   |   Acute Respiratory Distress Syndrome   |   Acute tubular necrosis   |   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   |   Adactylia unilateral dominant   |   Adam complex familial   |   Adams Nance syndrome   |   Adams Oliver Syndrome   |   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   |   Adenoma of the adrenal gland   |   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   |   Adolescent benign focal crisis   |   Adrenal adenoma, familial   |   Adrenal cancer   |   Adrenal disorder   |   Adrenal gland hyperfunction   |   Adrenal gland hypofunction   |   Adrenal hyperplasia   |   Adrenal Hyperplasia, Congenital (General)   |   Adrenal hypertension   |   Adrenal hypoplasia   |   Adrenal hypoplasia congenital, X-linked   |   Adrenal incidentaloma   |   Adrenal insufficiency   |   Adrenal macropolyadenomatosis   |   Adrenal medulla neoplasm   |   Adrenocortical carcinoma   |   Adrenogenital syndrome   |   Adrenoleukodystrophy   |   Adrenoleukodystrophy, autosomal, neonatal form   |   Adrenoleukodystrophy, X-linked   |   Adrenomyodystrophy   |   Adult onset Still's disease   |   Adult spinal muscular atrophy   |   Adult syndrome   |   Aerophobia   |   Afibrinogenemia, Congenital   |   Agammaglobulinemias, Primary   |   Aganglionosis, total intestinal   |   Ageing   |   Agenesis of Corpus Callosum   |   Aggressive fibromatosis   |   Agnathia holoprosencephaly situs inversus   |   Agnosia, Primary Visual   |   Agoraphobia   |   Agranulocytosis, Acquired   |   Agrizoophobia   |   Agyria pachygyria polymicrogyria   |   Agyria-pachygyria type 1   |   Agyrophobia   |   Ahumada-Del Castillo Syndrome   |   Aicardi Syndrome   |   Aicardi-Goutieres syndrome   |   Aichmophobia   |   AIDS (Acquired Immune Deficiency Syndrome)   |   AIDS Dementia Complex   |   AIDS Dysmorphic Syndrome   |   Ainhum   |   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   |   Alagille Syndrome   |   Alagille-Watson syndrome (AWS)   |   Alar nasal cartilages coloboma of telecanthus   |   Albers-Schonberg disease   |   Albinism   |   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   |   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   |   Aldolase A deficiency   |   Aldred syndrome   |   Alektorophobia   |   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   |   Alliumphobia   |   Allodoxaphobia   |   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   |   Alopecia universalis onychodystrophy vitiligo   |   Alopecia, epilepsy, pyorrhea, mental subnormality   |   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   |   Alport syndrome macrothrombocytopenia   |   Alport syndrome, dominant type   |   Alport syndrome, recessive type   |   Alstrom Syndrome   |   Alternating hemiplegia   |   Alternating Hemiplegia of Childhood   |   Aluminium lung   |   Alveolar Capillary Dysplasia   |   Alveolar echinococcosis   |   Alveolar Soft Part Sarcoma   |   Alveolitis, Extrinsic Allergic   |   Alves Dos Santos Castello syndrome   |   Alzheimer disease, familial   |   Alzheimer's Disease   |   Amathophobia   |   Amaurosis   |   Amaurosis congenita of Leber   |   Amaurosis congenita of Leber, type 1   |   Amaurosis congenita of Leber, type 2   |   Amaurosis hypertrichosis   |   Amaxophobia   |   Amblyopia   |   Ambral syndrome   |   Ambras syndrome   |   Ambulophobia   |   Amegakaryocytic thrombocytopenia   |   Amelia cleft lip palate hydrocephalus iris coloboma   |   Amelia facial dysmorphism   |   Amelia X linked   |   Ameloblastoma   |   Amelogenesis Imperfecta   |   Amelogenesis Imperfecta hypomaturation type   |   Amelogenesis imperfecta local hypoplastic form   |   Amelogenesis imperfecta nephrocalcinosis   |   Ameloonychohypohidrotic syndrome   |   Amenorrhea, Primary   |   Amenorrhea-Galactorrhea Syndrome   |   American trypanosomiasis   |   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   |   Amyloidosis of gingiva and conjunctiva mental retardation   |   Amyloidosis, Familial   |   Amylopectinosis   |   Amyoplasia   |   Amyoplasia mandibulofacial dysostosis   |   Amyotonia congenita   |   Amyotrophic Lateral Sclerosis   |   Anablephobia   |   Anaphylaxis   |   Anaplastic thyroid cancer   |   Andersen Disease (GSD IV)   |   Andre syndrome   |   Androgen insensitivity syndrome (AIS)   |   Androgen Insensitivity Syndrome, Partial   |   Anemia   |   Anemia sideroblastic spinocerebellar ataxia   |   Anemia, Blackfan Diamond   |   Anemia, Fanconi's   |   Anemia, Hemolytic, Acquired Autoimmune   |   Anemia, Hemolytic, Cold Antibody   |   Anemia, Hemolytic, Warm Antibody   |   Anemia, Hereditary Nonspherocytic Hemolytic   |   Anemia, Hereditary Spherocytic Hemolytic   |   Anemia, Hypoplastic, Congenital   |   Anemia, Megaloblastic   |   Anemia, Pernicious   |   Anemias, Sideroblastic   |   Anemophobia   |   Anencephaly   |   Anencephaly spina bifida X linked   |   Aneurysm   |   Aneurysm   |   Aneurysm of sinus of Valsalva   |   Aneurysm, intracranial berry   |   Angel shaped phalangoepiphyseal dysplasia   |   Angelman Syndrome   |   Angioedema, Hereditary   |   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   |   Anguillulosis   |   Aniridia   |   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   |   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   |   Annular constricting bands   |   Annular pancreas   |   Annuloaortic ectasia   |   Anodontia   |   Anonychia ectrodactyly   |   Anonychia microcephaly   |   Anonychia onychodystrophy   |   Anonychia onychodystrophy brachydactyly type B   |   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   |   Anotia facial palsy cardiac defect   |   Ansell Bywaters Elderking syndrome   |   Anterior horn disease   |   Anterior pituitary insufficiency, familial   |   Anthophobia   |   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, congenital   |   Antisocial Personality Disorder   |   Antisynthetase syndrome   |   Antithrombin deficiency, congenital   |   Antithrombin III Deficiency   |   Antley Bixler Syndrome   |   Antlophobia   |   Anton's syndrome   |   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   |   APECED Syndrome   |   Apert like polydactyly syndrome   |   Apert Syndrome   |   Aphalangia hemivertebrae   |   Aphalangia syndactyly microcephaly   |   Aphthous stomatitis   |   Apiphobia   |   Aplasia cutis autosomal recessive   |   Aplasia Cutis Congenita   |   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 myopia   |   Aplasia/hypoplasia of pelvis, femur, fibula, and ulna with abnormal digits and nails   |   Aplastic anemia   |   Apnea, Infantile   |   Apnea, Sleep   |   Apo A-I deficiency   |   Apolipoprotein C-II deficiency   |   Apparent mineralocorticoid excess   |   Appendicitis   |   Apraxia   |   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   |   Arachnoid Cysts   |    Arachnoiditis   |   Arakawa'sa syndrome II   |   Arbovirosis   |   Arc syndrome   |   AREDYLD   |   Aredyld syndrome   |   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   |   Arrhinia   |   Arrhythmogenic right ventricular dysplasia   |   Arroyo Garcia Cimadevilla syndrome   |   Arrythmogenic right ventricular dysplasia, familial   |   Arterial calcification of infancy   |   Arterial dysplasia   |   Arterial tortuosity   |   Arteriovenous Malformation   |   Arteritis   |   Arteritis, Giant Cell   |   Arteritis, Takayasu   |   Arthritis   |   Arthritis short stature deafness   |   Arthritis, Infectious   |   Arthritis, Juvenile Rheumatoid   |   Arthritis, Psoriatic   |   Arthrogryposis   |   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   |   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   |   Asbestosis   |   Ascariasis   |   Ascher's Syndrome   |   Aseptic meningitis   |   Asherman's Syndrome   |   Aspartylglycosaminuria   |   Asperger's Syndrome   |   Aspergillosis   |   Asphyxia neonatorum   |   Asthenia   |   Asthenia   |   Asthenophobia   |   Asthma   |   Astrocytoma   |   Astrocytoma, Malignant   |   Asymmetric septal hypertrophy   |   Ataxia Telangiectasia   |   Ataxia telangiectasia variant V1   |   Ataxia with Vitamin E Deficiency   |   Ataxia, Friedreich's   |   Ataxia, Hereditary, Autosomal Dominant   |   Ataxia, Marie's   |   Ataxiophobia   |   Ataxophobia   |   Atelectasis   |   Atelosteogenesis, type II   |   Athabaskan brain stem dysgenesis   |   Atherosclerosis   |   Athetosis   |   Atopic Dermatitis   |   Atresia of small intestine   |   Atrial myxoma, familial   |   Atrial Septal Defects   |   Atrioventricular fistula   |   Atrioventricular Septal Defect   |   Atrophoderma of Pierini and Pasini   |   Atrophy   |   ATR-X   |   Attention Deficit Hyperactivity Disorder   |   Attenuated FAP   |   Atychiphobia   |   Atypical Hemolytic Uremic Syndrome   |   Atypical lipodystrophy   |   Atypical Mole Syndrome   |   Auditory Perceptual Disorder   |   Aughton syndrome   |   Ausems Wittebol Post Hennekam syndrome   |   Autism   |   Autoimmune hemolytic anemia   |   Autoimmune hepatitis   |   Autoimmune peripheral neuropathy   |   Autoimmune Polyendocrine Syndrome Type II   |   Autoimmune Thyroiditis   |   Automysophobia   |   Autonomic dysfunction   |   Autonomic nervous system diseases   |   Axial mesodermal dysplasia spectrum   |   Axial osteomalacia   |   Axial osteosclerosis   |   Ayazi syndrome   |