Condiciones contempladas por la Dra. Rachael |
||
---|---|---|
Incluidas actualmente (600) | Bajo consideración (550) | No incluidas (52) |
Crohn's Disease | Great vessels transposition | |
Acromegaly | Proteus syndrome | |
Lyme Disease | Neurofibromatosis | |
Meningitis | Monoclonal Gammopathy of Undetermined Significance | |
Porphyria | Oculocutaneous albinism | |
Dercum's Disease | streptococci | |
Multiple Sclerosis | Meyer Dysplasia | |
Neuromyelitis Optica (Devic Disease) | Staphylococci | |
Pulmonary Arterial Hypertension | Fitzsimmons Walson Mellor syndrome | |
Hemophilia | Fibrochondrogenesis | |
Guillain-Barre syndrome | pneumococci | |
Madelung’s disease | astroblastoma | |
Marfan syndrome | Actinic lichen planus | |
Parsonage Turner Syndrome | Aldred syndrome | |
Congenital Contractural Arachnodactyly | Ameloblastoma | |
Addison’s Disease | Apocrine carcinoma | |
Ramsay Hunt Syndrome | Boudhina Yedes Khiari syndrome | |
Tay-Sachs Disease | Calvarial hiperostosis | |
Sandhoff Disease | Chancroid | |
Kufs Disease | Hydrops fetalis | |
Kawasaki Disease | Nodding syndrome | |
Toxic Shock Syndrome | Papilledema | |
Wegener’s Granulomatosis | Renal oncocytoma | |
Goodpasture Syndrome | Somatostatinoma | |
Cushing Syndrome | Familial streblodactyly | |
Mitral Valve Prolapse Syndrome | Cartwright Nelson Fryns syndrome | |
Myasthenia Gravis | Angiomyomatous Hamartoma | |
Lambert-Eaton Myasthenic Syndrome | Diphallia | |
Reflex Sympathetic Dystrophy Syndrome | Duplication of leg mirror foot | |
Erythromelalgia | Pheochromocytoma | |
Polycythemia Vera | Pinta | |
Chronic Inflammatory Demyelinating Polyneuropathy | Kleiner Holmes syndrome | |
Amyloidosis | Hemolytic anemia lethal congenital nonspherocytic with genital and other abnormalities | |
Multiple Myeloma | Potato nose | |
Whipple Disease | Sialadenitis | |
Osteomyelitis | Sitosterolemia | |
Waldenström's Macroglobulinemia | Cicatricial Alopecia | |
Maple Syrup Urine Disease | Oslam syndrome | |
Balantidiasis | Renoprival hypertension | |
Pantothenate kinase-associated neurodegeneration (PKAN) | Tetanus | |
Methylmalonic Acidemia | Histidinemia | |
Winchester Syndrome | Dwarfism Levi type | |
Farber’s Disease | Dystelephalangy | |
Moyamoya Disease | Scurvy | |
Sickle Cell Disease | Breast cancer, familial | |
Hereditary Spherocytic Hemolytic Anemia | Stargardt disease | |
Restless Legs syndrome | Alopecia Areata | |
Refsum Disease | Melanoma, familial | |
Adrenoleukodystrophy | Diaphragmatic hernia, congenital | |
Metachromatic Leukodystrophy | Oesophageal atresia | |
Alexander Disease Type I | Familial adenomatous polyposis | |
Alexander Disease Type II | Kostmann disease | |
Ogilvie syndrome | ||
Chronic Intestinal Pseudo-obstruction | ||
Achondrogenesis | ||
Kniest Dysplasia | ||
Campomelic Syndrome | ||
Hypophosphatasia | ||
Morquio Syndrome | ||
Osteogenesis Imperfecta Type I | ||
Osteogenesis Imperfecta Type II | ||
Osteogenesis Imperfecta Type III | ||
Osteogenesis Imperfecta Type IV | ||
Mumps | ||
Leigh Syndrome | ||
Gilbert syndrome | ||
Dubin Johnson Syndrome | ||
Crigler Najjar Syndrome | ||
Babesiosis | ||
TORCH Syndrome | ||
Vogt-Koyanagi-Harada Disease | ||
Usher Syndrome Type I | ||
Usher Syndrome Type II | ||
Usher Syndrome Type III | ||
Usher Syndrome Type IV | ||
Alström Syndrome | ||
Retinitis Pigmentosa | ||
Leber's Congenital Amaurosis | ||
Joubert Syndrome | ||
Meckel Syndrome | ||
Dubowitz Syndrome | ||
Noonan Syndrome | ||
Turner Syndrome | ||
Klinefelter Syndrome | ||
Kallmann Syndrome | ||
Acoustic Neuroma | ||
Ménière’s Disease | ||
Creutzfeldt Jakob Disease | ||
Gerstmann Syndrome | ||
Kikuchi’s Disease | ||
Hodgkin’s Disease | ||
Köhler Disease | ||
Tarsal Tunnel syndrome | ||
Sweet Syndrome | ||
Schnitzler Syndrome | ||
Familial Mediterranean Fever | ||
Familial Cold Autoinflammatory Syndrome | ||
Cogan-Reese Syndrome | ||
Chandler’s Syndrome | ||
Essential Iris Atrophy | ||
Rieger Syndrome | ||
Carnosinemia | ||
Phenylketonuria | ||
Cerebral Palsy: Tetrahydrobiopterin Deficiency | ||
Progressive Multifocal Leukoencephalopathy | ||
Paget’s disease | ||
Pallister Hall Syndrome | ||
Aarskog Syndrome | ||
Abetalipoproteinemia | ||
Ablepharon-Macrostomia Syndrome | ||
Acquired Aplastic Anemia | ||
Aceruloplasminemia | ||
Acidemia Isovaleric | ||
Yellow Nail syndrome | ||
Weil Syndrome | ||
Adult Neuronal Ceroid Lipofuscinosis | ||
Unverricht-Lundborg Disease | ||
Legg Calvé Perthes Disease | ||
Spondyloepiphyseal Dysplasia Tarda | ||
Fitz Hugh Curtis Syndrome | ||
Cholecystitis | ||
Fox Fordyce Disease | ||
Hidradenitis Suppurativa | ||
Keratosis Follicularis | ||
Fibrodysplasia Ossificans Progressiva | ||
Glucose Transporter Type 1 Deficiency Syndrome | ||
Lymphangioleiomyomatosis | ||
Langerhans Cell Histiocytosis | ||
Rosai-Dorfman Disease | ||
Erdheim Chester Disease | ||
Erysipelas | ||
Essential Tremor | ||
Q fever | ||
Epidermolysis Bullosa | ||
Peeling Skin Syndrome | ||
Leber Hereditary Optic Neuropathy | ||
Fatal Familial Insomnia | ||
Dupuytren’s Contracture | ||
Dravet Syndrome Spectrum | ||
Duchenne Muscular Dystrophy | ||
Dysautonomia, Familial | ||
Dyskeratosis Congenita | ||
L1 Syndrome | ||
Lenz Microphthalmia Syndrome | ||
Nance-Horan Syndrome | ||
Oculo-Dento-Digital Dysplasia | ||
Hartnup Disease | ||
Hajdu Cheney Syndrome | ||
Hantavirus Pulmonary Syndrome | ||
Henoch-Schönlein Purpura | ||
Hereditary Coproporphyria | ||
Hermansky Pudlak Syndrome | ||
Holt Oram Syndrome | ||
Hyperekplexia | ||
Hyperlipoproteinemia Type III | ||
Hypochondroplasia | ||
Hypohidrotic Ectodermal Dysplasia | ||
Amyotrophic Lateral Sclerosis | ||
Lipoprotein Lipase Deficiency | ||
Choroideremia | ||
Transthyretin Amyloidosis | ||
Susac’s syndrome | ||
Huntington disease | ||
Urbach-Wiethe Disease | ||
Hemochromatosis | ||
Hemophagocytic Lymphohistiocytosis | ||
Friedreich’s Ataxia | ||
Mastocytosis | ||
Bardet-Biedl Syndrome | ||
Gaucher disease | ||
Senior-Loken Syndrome | ||
Muckle-Wells Syndrome | ||
Churg-Strauss syndrome | ||
Sennetsu Fever | ||
Seckel Syndrome | ||
Homocystinuria | ||
Trisomy 13 Syndrome | ||
Bloom Syndrome | ||
Still’s disease | ||
Trigeminal Neuralgia | ||
Hailey-Hailey Disease | ||
Charcot-Marie-Tooth Disease | ||
Acid sphingomyelinase deficiency | ||
Gerstmann-Sträussler-Scheinker Disease | ||
Tumor Necrosis Factor Receptor-Associated Periodic Syndrome | ||
Moebius syndrome | ||
CHARGE Syndrome | ||
Primary Sclerosing Cholangitis | ||
Achondroplasia | ||
Primary Myelofibrosis | ||
Kugelberg Welander Syndrome | ||
Oral-Facial-Digital Syndrome | ||
Essential Thrombocythemia | ||
Chronic Erosive Gastritis | ||
Chronic Infantile Neurological Cutaneous Articular (CINCA) syndrome | ||
Dejerine-Sottas disease | ||
Human Granulocytic Ehrlichiosis (HGE) | ||
Costello syndrome | ||
Acute flaccid myelitis (AFM) | ||
Klippel-Trenaunay Syndrome | ||
Incontinentia pigmenti | ||
Aicardi syndrome | ||
CADASIL | ||
Li-Fraumeni syndrome | ||
Castleman disease | ||
Kabuki syndrome | ||
Cerebrotendinous xanthomatosis | ||
Larsen syndrome | ||
Kearns-Sayre syndrome | ||
Cockayne syndrome | ||
Cohen syndrome | ||
Silver-Russell syndrome | ||
Denys-Drash syndrome | ||
CHILD syndrome | ||
Waardenburg syndrome | ||
Schinzel-Giedion syndrome | ||
Pallister-Killian syndrome | ||
Systemic Capillary Leak Syndrome | ||
Acrocallosal syndrome, Schinzel type | ||
Alpha Thalassemia X-linked Intellectual Disability Syndrome | ||
McCune Albright syndrome | ||
Job syndrome | ||
Alpha-1 Antitrypsin Deficiency | ||
Chromosome 22q11.2 Deletion Syndrome | ||
Treacher Collins Syndrome | ||
Tumor-induced osteomalacia | ||
Parry Romberg Syndrome | ||
Idiopathic Pulmonary Fibrosis | ||
Macrophagic myofasciitis | ||
Congenital Disorders of Glycosylation | ||
Coffin Siris Syndrome | ||
Brugada Syndrome | ||
Tetralogy of Fallot | ||
Scleroderma | ||
Dystonia | ||
Mantle Cell Lymphoma | ||
Narcolepsy | ||
Neurofibromatosis 1 | ||
Coffin-Lowry Syndrome | ||
Hereditary Hemorrhagic Telangiectasia | ||
Dermatitis Herpetiformis | ||
Duodenal Atresia | ||
Ehlers Danlos Syndromes | ||
Hirschsprung disease | ||
Hereditary Spherocytosis | ||
MELAS syndrome | ||
Lennox-Gastaut Syndrome | ||
Fragile X Syndrome | ||
Stickler Syndrome | ||
Williams Syndrome | ||
Spinal muscular atrophy | ||
Tuberous Sclerosis | ||
Rett syndrome | ||
Von Hippel-Lindau Disease | ||
Mucopolysaccharidosis | ||
Polymyositis and Necrotizing Myopathy | ||
Cystic fibrosis | ||
Mevalonate Kinase Deficiency | ||
Blau syndromes | ||
Fabry Disease | ||
Sialidosis | ||
I-cell disease | ||
Pseudo-Hurler polydystrophy | ||
Mucolipidosis IV | ||
Pompe disease | ||
Marshall Syndrome | ||
Wolf-Hirschhorn Syndrome | ||
Diamond Blackfan Anemia | ||
Lesch-Nyhan syndrome | ||
Prader-Willi Syndrome | ||
Smith-Magenis Syndrome | ||
Angelman syndrome | ||
Ataxia with Vitamin E Deficiency | ||
Galactosemia | ||
Glycogen Storage Disease Type III | ||
Severe Chronic Neutropenia | ||
Gastrointestinal Stromal Tumors | ||
Multiple Endocrine Neoplasia Type 1 | ||
VACTERL association | ||
Behçet's syndrome | ||
Congenital central hypoventilation syndrome | ||
Phelan-McDermid syndrome | ||
Optic Nerve Hypoplasia | ||
Ocular Albinism | ||
Chediak Higashi Syndrome | ||
Apert Syndrome | ||
Landau Kleffner Syndrome | ||
Trisomy 18 | ||
Beckwith-Wiedemann Syndrome | ||
Hereditary Fructose Intolerance | ||
Primary ciliary dyskinesia | ||
Progressive supranuclear palsy | ||
Juvenile CLN3 disease | ||
Classic infantile CLN1 disease | ||
Myotonic Dystrophy | ||
Propionic Acidemia | ||
Oculo-Auriculo-Vertebral Spectrum | ||
ADNP Syndrome | ||
Menkes Disease | ||
POEMS syndrome | ||
Pyoderma gangrenosum | ||
Cystinosis | ||
Lowe syndrome | ||
Kennedy Disease | ||
Dermatomyositis | ||
Variegate Porphyria | ||
Empty Sella Syndrome | ||
Familial Adenomatous Polyposis | ||
Ewing Sarcoma | ||
Stargardt disease | ||
Rubinstein-Taybi syndrome | ||
Wilson disease | ||
Biotinidase deficiency | ||
Nemaline Myopathy | ||
Cryptococcosis | ||
Hypokalemic periodic paralysis | ||
Emery Dreifuss Muscular Dystrophy | ||
Ataxia Telangiectasia | ||
Okihiro syndrome | ||
Pyknodysostosis | ||
Osteopetrosis | ||
Lewis-Sumner syndrome | ||
Anemia, Hemolytic, Cold Antibody | ||
Jansky-Bielschowsky disease | ||
Sarcoidosis | ||
Plasma cell leukemia | ||
Freeman-Sheldon syndrome | ||
Gastritis, Giant Hypertrophic | ||
Rocky Mountain Spotted Fever | ||
Wernicke-Korsakoff Syndrome | ||
Human Monocytic Ehrlichiosis (HME) | ||
Bell’s Palsy | ||
Leukodystrophy, Krabbe’s | ||
Beta Thalassemia | ||
Alpha Thalassemia | ||
Glutaric Aciduria Type I | ||
Glutaric Aciduria Type II | ||
Astrocytoma | ||
Pelizaeus-Merzbacher disease | ||
Acquired immune deficiency syndrome | ||
Nephronophthisis | ||
COACH syndrome | ||
Lymphatoid granulomatosis | ||
Idiopathic pulmonary hemosiderosis | ||
Polyarteritis nodosa | ||
Multifocal motor neuropathy | ||
Smith-Lemli-Opitz (SLO) syndrome | ||
Multicentric osteolysis, nodulosis and arthropathy | ||
Burkitt’s lymphoma | ||
Lafora disease | ||
Spondyloepiphyseal Dysplasia, Congenital | ||
Dyggve Melchior Clausen syndrome | ||
Chronic inflammatory demyelinating polyradiculoneuropathy | ||
Central Pain Syndrome | ||
Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) | ||
Erythema Multiforme | ||
Cole Carpenter syndrome | ||
Dekaban-Arima syndrome | ||
Chronic Myelogenous Leukemia | ||
Meningioma | ||
Frontotemporal dementia | ||
Jumping Frenchmen of Maine | ||
Townes Brocks Syndrome | ||
Ivemark syndrome | ||
Chromosome 10, Distal Trisomy 10q | ||
Dominant Multiple Epiphyseal Dysplasia | ||
Primary Biliary Cholangitis | ||
Canavan disease | ||
Neuropathy ataxia retinitis pigmentosa syndrome | ||
Hereditary Neuralgic Amyotrophy | ||
Familial multiple lipomatosis | ||
Multiple system atrophy | ||
Schmidt syndrome | ||
Fetal alcohol syndrome | ||
Fanconi Anemia | ||
Pachydermoperiostosis | ||
Cardiofaciocutaneous syndrome | ||
Neurofibromatosis-Noonan syndrome | ||
Cyclic vomiting syndrome | ||
Cone dystrophy | ||
Anemia, Hereditary Nonspherocytic Hemolytic | ||
Zellweger Spectrum Disorders | ||
Eosinophilic Fasciitis | ||
Ocular Motor Apraxia, Cogan Type | ||
Familial Hypophosphatemia | ||
Thyroid Cancer | ||
Chiari Malformations | ||
Ectodermal Dysplasias | ||
X-linked adrenal hypoplasia congenita | ||
Congenital adrenal hyperplasia | ||
Psittacosis | ||
Iris hypoplasia and glaucoma | ||
Urea cycle disorders | ||
Primary Mitochondrial Myopathies | ||
Severe Combined Immunodeficiency | ||
Agammaglobulinemia | ||
Rasmussen Encephalitis | ||
Congenital Muscular Dystrophy | ||
Mucopolysaccharidosis Type III | ||
Langer Giedion Syndrome | ||
Alkaptonuria | ||
Nakajo syndrome | ||
Osteosarcoma | ||
hypereosinophilic syndrome | ||
Blastomycosis | ||
Lichtenstein syndrome | ||
Cherubism | ||
Insulinoma | ||
Madelung deformity | ||
Bassoe syndrome | ||
Acromicric dysplasia | ||
Tetraploidy | ||
Syringomyelia | ||
Swyer syndrome | ||
Acrodysostosis | ||
Anorchia | ||
Atransferrinemia | ||
Barakat syndrome | ||
Cysticercosis | ||
Cystinuria | ||
Danon disease | ||
Darier disease | ||
Desmoid tumor | ||
Dirofilariasis | ||
DOOR syndrome | ||
Feingold syndrome | ||
Flynn Aird syndrome | ||
Frasier syndrome | ||
Frias syndrome | ||
Fucosidosis | ||
Wagner syndrome | ||
Warfarin syndrome | ||
West syndrome | ||
Mycetoma | ||
Muenke Syndrome | ||
Micro syndrome | ||
Martsolf syndrome | ||
Kanzaki disease | ||
Griscelli syndrome | ||
Dravet syndrome | ||
Diencephalic syndrome | ||
Dent disease | ||
Dengue fever | ||
Cyclic neutropenia | ||
Cutis marmorata telangiectatica congenita | ||
Cutis laxa | ||
Takayasu arteritis | ||
TAR syndrome | ||
Tangier disease | ||
Piebaldism | ||
Perrault syndrome | ||
Pearson syndrome | ||
Ollier disease | ||
Oliver syndrome | ||
Norrie disease | ||
Mullerian aplasia | ||
Mulibrey Nanism | ||
Milroy disease | ||
Miller syndrome | ||
Microscopic polyangiitis | ||
Metatropic dysplasia | ||
Malakoplakia | ||
Listeria infection | ||
LEOPARD syndrome | ||
Jeune syndrome | ||
Hypothalamic hamartomas | ||
Hypomelanosis of Ito | ||
Heavy metal poisoning | ||
Gomez Lopez Hernandez syndrome | ||
Gitelman syndrome | ||
Kyphomelic dysplasia | ||
Rhizomelic chondrodysplasia punctata | ||
Free sialic acid storage disease | ||
Frontonasal dysplasia | ||
Aagenaes syndrome | ||
Acrodermatitis enteropathica | ||
Adie syndrome | ||
Lujan syndrome | ||
Dysferlinopathy | ||
Björnstad Syndrome | ||
Fraser Syndrome | ||
Genoa syndrome | ||
Krabbe disease | ||
Harding ataxia | ||
Wagner syndrome | ||
IRVAN syndrome | ||
Buerger’s Disease | ||
Mevalonic aciduria | ||
Cat scratch disease | ||
Evans Syndrome | ||
Neu Laxova Syndrome | ||
Antley-Bixler Syndrome | ||
Felty Syndrome | ||
Filippi Syndrome | ||
Hemi 3 syndrome | ||
Pachygyria | ||
Degos disease | ||
Rubella, Congenital | ||
Botulism | ||
Tyrosine Hydroxylase Deficiency | ||
Hereditary Angioedema | ||
Non-24-Hour Sleep-Wake Disorder | ||
Barth syndrome | ||
Kaposi sarcoma | ||
Sturge-Weber Syndrome | ||
Keratoconus | ||
Catel-Manzke syndrome | ||
Arthrogryposis Multiplex Congenita | ||
Spinal Muscular Atrophy with Respiratory Distress | ||
Duane syndrome | ||
Limb-Girdle Muscular Distrophies | ||
Alternating Hemiplegia of Childhood | ||
Filippi syndrome | ||
Focal dermal hipoplasia | ||
Fountain syndrome | ||
Hydranencephaly | ||
IgA nephropathy | ||
Inclusion body myositis | ||
Melkersson-Rosenthal syndrome | ||
Glanzmann Thrombasthenia | ||
Nakajo-Nishimura syndrome | ||
Ichthyosis, Netherton Syndrome | ||
Simian B Virus Infection | ||
Primary Visual Agnosia | ||
Caudal Regression Syndrome | ||
Graves’ Disease | ||
Blue diaper syndrome | ||
Fryns Syndrome | ||
Hanhart syndrome | ||
Antiphospholipid syndrome | ||
Sutton Disease II | ||
Physical Allergy Urticaria | ||
Snyder-Robinson Syndrome | ||
Sotos syndrome | ||
Meige Syndrome | ||
Banti’s Syndrome | ||
Bowenoid Papulosis | ||
Brown Syndrome | ||
Seatworm Infection | ||
Fascioliasis | ||
Meleda Disease | ||
Mikulicz Syndrome | ||
Optic Nerve Papillitis | ||
Papillon-Lefèvre Syndrome | ||
Poland Syndrome | ||
Potter syndrome | ||
Proctitis | ||
Pyruvate Kinase Deficiency | ||
Radiation Sickness | ||
Reye Syndrome | ||
Renal Glycosuria | ||
Adenylosuccinase deficiency | ||
Alport syndrome | ||
Bronchiolitis Obliterans Organizing Pneumonia | ||
Cantu syndrome | ||
Carney triad | ||
Neonatal progeroid syndrome | ||
Peutz-Jeghers syndrome | ||
Retinoschisis | ||
Kernicterus | ||
Growth Hormone Insensitivity | ||
Sporadic Porencephaly | ||
Nail-patella Syndrome | ||
Transverse Myelitis | ||
Retroperitoneal Fibrosis | ||
Fibrosing Mediastinitis | ||
Alagille Syndrome | ||
Tarlov Cysts | ||
Pityriasis Rubra Pilaris | ||
Erythrokeratoderma | ||
Hereditary mucoepithelial dysplasia | ||
Emanuel syndrome | ||
Central Core Disease | ||
Gastroparesis | ||
Acute disseminated encephalomyelitis | ||
Chronic lymphocytic leukemia | ||
Riboflavin Transporter Deficiency | ||
Nonketotic Hyperglycinemia | ||
Hydrocephalus | ||
Congenital Generalized Lipodystrophy | ||
Bartonellosis | ||
Acquired Lipodystrophy | ||
Ulcerative Colitis | ||
Infective Endocarditis | ||
Leptospirosis | ||
Systemic Scleroderma | ||
Hallermann Streiff Syndrome | ||
Freiberg’s Disease | ||
Smith Lemli Opitz Syndrome | ||
Dandy-Walker Malformation | ||
Familial Hypophosphatemia | ||
Corticobasal Degeneration | ||
Rabson-Mendenhall Syndrome | ||
Obesity due to congenital leptin deficiency | ||
Psoriatic juvenile idiopathic arthritis | ||
Thoracic Outlet Syndrome | ||
Leri Pleonosteosis | ||
Chromosome 14 Ring | ||
Vitamin D Deficiency Rickets | ||
Short Bowel Syndrome |
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