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Medical Wikipedia

Ebola virus disease

Ectopic pregnancy

Ectrodactyly–ectodermal dysplasia–cleft syndrome

Ehlers–Danlos syndrome

Eisenmenger's syndrome

Elective mutism

Elejalde syndrome

Proteus syndrome

Emery–Dreifuss muscular dystrophy

Empty sella syndrome

Encephalitis lethargica

Encephalomyelitis

Sturge–Weber syndrome

Enchondromatosis

Endocardial fibroelastosis

Endometrial stromal sarcoma

Hypereosinophilic syndrome

Enolase deficiency

Entomophthoramycosis

Bothrops lanceolatus

Eosinophilia–myalgia syndrome

Eosinophilic cystitis

Eosinophilic fasciitis

Eosinophilic gastroenteritis

Eosinophilic granuloma

Eosinophilic folliculitis

Fear of daylight

Primitive neuroectodermal tumor

Epidermodysplasia verruciformis

Epidermolysis bullosa acquisita

Junctional epidermolysis bullosa (medicine)

Epidermolysis bullosa

Epidermolytic hyperkeratosis

Epilepsia partialis continua

Benign familial neonatal seizures

Absence seizure

Progressive myoclonus epilepsy

Galactose epimerase deficiency

Pacman dysplasia

Epithelial-myoepithelial carcinoma

Erythropoietic protoporphyria

Infectious mononucleosis

Erdheim–Chester disease

Erosive pustular dermatitis of the scalp

Erythema multiforme

Erythema nodosum

Erythromelalgia

Erythroblastopenia

Erythrokeratodermia with ataxia

Erythrokeratodermia variabilis

Keratolytic winter erythema

Erythroplasia of Queyrat

Pathogenic Escherichia coli

Esophageal atresia

Esophageal cancer

Esophageal varices

Essential fatty acid

Essential hypertension

Thrombocytopenia

Essential thrombocythaemia

Esthesioneuroblastoma

Organic acidemia

Ewing's sarcoma

Serpentine fibula-polycystic kidney syndrome

Hereditary multiple exostoses

Experimental autoimmune encephalomyelitis

Exploding head syndrome

Bladder exstrophy

Movement disorder

Seaver Cassidy syndrome

Facial nerve paralysis

Facioscapulohumeral muscular dystrophy

Factor V Leiden

Factor XIII deficiency

Multiple epiphyseal dysplasia

Tetralogy of Fallot

Transthyretin-related hereditary amyloidosis

Familial aortic dissection

Colorectal cancer

Familial dysautonomia

Lipoprotein lipase deficiency

Familial hypertriglyceridemia

Hypopituitarism

Familial Mediterranean fever

Periodic paralysis

Treacher Collins syndrome

Catecholaminergic polymorphic ventricular tachycardia

Fanconi syndrome

Fatal familial insomnia

Fazio–Londe disease

Febrile seizure

Fechtner syndrome

Feingold syndrome

Felty's syndrome

Female sexual arousal disorder

Femur fibula ulna syndrome

Congenital cytomegalovirus infection

Fetal hydantoin syndrome

Hydrops fetalis

Fetal warfarin syndrome

Fibrochondrogenesis

Fibromuscular dysplasia

Idiopathic pulmonary fibrosis

Fibrous dysplasia of bone

Fibrodysplasia ossificans progressiva

Lattice corneal dystrophy

Fish-eye disease

Fissured tongue

Fitz-Hugh–Curtis syndrome

Fitzsimmons–Guilbert syndrome

Pseudomonas oryzihabitans

Necrotizing fasciitis

Floating-Harbor syndrome

Endosalpingiosis

Flynn–Aird syndrome

Focal dermal hypoplasia

Focal facial dermal dysplasia

Foix–Chavany–Marie syndrome

Foix–Alajouanine syndrome

Follicular lymphoma

Glycogen storage disease type III

Foreign accent syndrome

Fountain syndrome

Fournier gangrene

Fox–Fordyce disease

Fragile X syndrome

Franceschetti–Klein syndrome

Hallermann–Streiff syndrome

Fraser syndrome

Frasier syndrome

Infantile free sialic acid storage disease

Freeman–Sheldon syndrome

Freiberg disease

Frey's syndrome

Friedreich's ataxia

Adiposogenital dystrophy

Frontonasal dysplasia

Hereditary fructose intolerance

Fructose 1,6-bisphosphatase

Essential fructosuria

Fukuyama congenital muscular dystrophy

Fumarase deficiency

Neuroendocrine tumor

List of diseases (G)

Galactokinase deficiency

Galactorrhea hyperprolactinemia

Morquio syndrome

Galactose-1-phosphate uridylyltransferase deficiency

Galloway Mowat syndrome

Hyperkalemic periodic paralysis

GM2 gangliosidoses

GM1 gangliosidoses

Ganser syndrome

Painful bruising syndrome

Nissen fundoplication

Gastric dumping syndrome

Gastric lymphoma

Gastrocutaneous syndrome

Gastrointestinal cancer

Gaucher's disease

Weill–Marchesani syndrome

Gender identity disorder

Miller syndrome

Generalized anxiety disorder

Thyroid hormone resistance

Generalised epilepsy

Koro (medicine)

Geographic tongue

Fetal trimethadione syndrome

Gerodermia osteodysplastica

Gerstmann syndrome

Gestational diabetes

Gestational pemphigoid

Gestational trophoblastic disease

Gianotti–Crosti syndrome

Giant axonal neuropathy

Giant-cell arteritis

Idiopathic giant-cell myocarditis

Congenital melanocytic nevus

Giant platelet disorder

Gilbert's syndrome

Tourette syndrome

Gitelman syndrome

Glanzmann's thrombasthenia

Glioblastoma multiforme

Gliomatosis cerebri

Glomerulonephritis

Glomerulosclerosis

Glucose-6-phosphate dehydrogenase deficiency

Glucose-galactose malabsorption

Glutaric aciduria type 1

Glutathione synthetase deficiency

Glycogen storage disease

Glycogen storage disease type I

Glycogen storage disease type VI

Phosphofructokinase deficiency

Glycogen storage disease type V

Glycogen storage disease type IV

Glycogen storage disease type 0

Goldenhar syndrome

Gonadal dysgenesis

Mixed gonadal dysgenesis

XY gonadal dysgenesis

Neisseria gonorrhoeae

Goodpasture syndrome

Gorham's disease

Gougerot–Blum syndrome

Graft-versus-host disease

Granuloma annulare

Lymphomatoid granulomatosis

Graves' disease

Gray platelet syndrome

Hydrops-ectopic calcification-moth-eaten skeletal dysplasia

Transient acantholytic dermatosis

Growth hormone deficiency

Guanidinoacetate methyltransferase deficiency

Hagemoser–Weinstein–Bresnick syndrome

Hailey–Hailey disease

Hairy cell leukemia

Hairy palms and soles

Black hairy tongue

Hajdu–Cheney syndrome

Pantothenate kinase-associated neurodegeneration

Hallucinogen persisting perception disorder

Nevus sebaceous

Hand, foot and mouth disease

Hand–Schüller–Christian disease

Tyrosinemia type II

Harlequin-type ichthyosis

Hartnup disease

Hashimoto's thyroiditis

Congenital self-healing reticulohistiocytosis

Hay–Wells syndrome

Aneurysm of heart

Myocardial infarction

Primary tumors of the heart

Heavy metal (chemistry)

Hemangioblastoma

Hemangioendothelioma

Kasabach–Merritt syndrome

Hemangiopericytoma

Hemifacial microsomia

Familial hemiplegic migraine

HFE hereditary haemochromatosis

Juvenile hemochromatosis

Haemochromatosis type 3

Hemoglobinopathy

Hemolytic-uremic syndrome

Hemophagocytic lymphohistiocytosis

Hantavirus hemorrhagic fever with renal syndrome

Bernard–Soulier syndrome

Hennekam syndrome

Heparin-induced thrombocytopenia

Hepatic encephalopathy

Hepatic veno-occlusive disease

Hepatocellular carcinoma

Hepatorenal syndrome

Type I tyrosinemia

Hereditary angioedema

Hereditary coproporphyria

Hereditary elliptocytosis

Hereditary hemorrhagic telangiectasia

Methemoglobinemia

Hereditary pancreatitis

Hereditary spastic paraplegia

Hermansky–Pudlak syndrome

Herpesviral encephalitis

Neonatal herpes simplex

Ramsay Hunt syndrome type II

Herpes of the eye

TNF receptor associated periodic syndrome

Sprengel's deformity

Dislocation of hip

Hip dysplasia (canine)

Hip dysplasia (human)

Junctional ectopic tachycardia

Orthomolecular medicine

Langerhans cell histiocytosis

Non-Langerhans cell histiocytosis

Histrionic personality disorder

Hodgkin's lymphoma

Smith–Fineman–Myers syndrome

Holocarboxylase synthetase deficiency

Holoprosencephaly

Holt–Oram syndrome

Horner's syndrome

Horseshoe kidney

Hot tub folliculitis

Howel–Evans syndrome

Ehrlichiosis ewingii infection

Human granulocytic anaplasmosis

Human monocytotropic ehrlichiosis

Hunter syndrome

Huntington's disease

Hurler syndrome

Hutchinson's teeth

Molar pregnancy

Hydranencephaly

Hydrolethalus syndrome

Primary hyperoxaluria

Hyperimmunoglobulin E syndrome

Hyper IgM syndrome

Hyperaldosteronism

Hyperandrogenism

Hypercementosis

Hypercholesterolemia

Hyperglycerolemia

Hyperglycinemia

Hyperhomocysteinemia

Hyper-IgD syndrome

Congenital hyperinsulinism

Hyperostosis frontalis interna

Hyperparathyroidism

Hyperphenylalaninemia

Pipecolic acidemia

Hyperprolinemia

Hypersensitivity

Type I hypersensitivity

Type II hypersensitivity

Type III hypersensitivity

Type IV hypersensitivity

Hypertensive retinopathy

Hyperthyroidism

Hypertriglyceridemia

Hypertryptophanemia

Hypervitaminosis A

Hypervitaminosis D

Hypervitaminosis E

Hypoactive sexual desire disorder

Hypoaldosteronism

Hypobetalipoproteinemia

Hypochondriasis

Hypochondrogenesis

Hypochondroplasia

Urticarial vasculitis

Hypohidrotic ectodermal dysplasia

Hypokalemic periodic paralysis

Hypokalemic sensory overstimulation

Hypolipoproteinemia

Prader–Willi syndrome

Hypoparathyroidism

Hypophosphatasia

X-linked hypophosphatemia

Hypoplastic left heart syndrome

Michels Caskey syndrome

Hypoprothrombinemia

Pallister–Hall syndrome

Tuber cinereum hamartoma

Hypoxia (medical)

Trichothiodystrophy

Immunodeficiency–centromeric instability–facial anomalies syndrome

Ichthyoallyeinotoxism

Ichthyosis bullosa of Siemens

Ruzicka Goerz Anton syndrome

Ichthyosis follicularis with alopecia and photophobia syndrome

Ichthyosis linearis circumflexa

Netherton syndrome

Juvenile osteoporosis

Idiopathic pulmonary haemosiderosis

Idiopathic sclerosing mesenteritis

Idiopathic thrombocytopenic purpura

Selective immunoglobulin A deficiency

Iminoglycinuria

Impossible syndrome

Inborn error of metabolism

Inborn errors of renal tubular transport

Urea cycle disorder

Incontinentia pigmenti

Incontinentia pigmenti achromians

Infant respiratory distress syndrome

Infantile digital fibromatosis

Epileptic spasms

Spinal muscular atrophies

Septic arthritis

Inflammatory breast cancer

Inguinal hernia

Intoxicative inhalant

Intraocular lymphoma

Interstitial cystitis

Whipple's disease

Intestinal pseudoobstruction

Intestinal spirochetosis

Cerebral arteriovenous malformation

Vertically transmitted infection

Iodine deficiency

Iridogoniodysgenesis, dominant type

Iron deficiency

Irritable bowel syndrome

Asplenia with cardiovascular anomalies

Jackson–Weiss syndrome

Jacobsen syndrome

Pachyonychia congenita

Jalili syndrome

Spinal muscular atrophy with progressive myoclonic epilepsy

Jansky–Bielschowsky disease

Japanese encephalitis

Spondylocostal dysostosis

Jervell and Lange-Nielsen syndrome

Asphyxiating thoracic dysplasia

Johanson–Blizzard syndrome

Johnson–Munson syndrome

Joubert syndrome

Jumping Frenchmen of Maine

Juvenile dermatomyositis

Lesch–Nyhan syndrome

Juvenile hyaline fibromatosis

Juvenile myoclonic epilepsy

Kabuki syndrome

Kallmann syndrome

Kaposi's sarcoma

Kapur–Toriello syndrome

Primary ciliary dyskinesia

Kaufman oculocerebrofacial syndrome

Kawasaki disease

Kearns–Sayre syndrome

Spinal and bulbar muscular atrophy

Keratoacanthoma

Keratoconjunctivitis sicca

Keratosis follicularis spinulosa decalvans

Keratosis pilaris

Seborrheic keratosis

Keutel syndrome

Anaplastic large-cell lymphoma

Keratitis–ichthyosis–deafness syndrome

Kikuchi disease

Kimura's disease

Malignant hyperthermia

Kjer's optic neuropathy

Kleine–Levin syndrome

Klippel–Trénaunay syndrome

Klumpke paralysis

Klüver–Bucy syndrome

Kniest dysplasia

Familial partial lipodystrophy

Kocher–Debre–Semelaigne syndrome

Köhler disease

Kohlschütter-Tönz syndrome

Korsakoff's syndrome

Kostmann syndrome

Kowarski syndrome

Peters-plus syndrome

Kyasanur forest disease

Lachiewicz–Sibley syndrome

Lambert–Eaton myasthenic syndrome

Lamellar ichthyosis

John Langdon Down

Langer–Giedion syndrome

Diffuse large B-cell lymphoma

Laryngeal cancer

Laryngeal cleft

Laryngeal papillomatosis

Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

Leber's hereditary optic neuropathy

Lecithin cholesterol acyltransferase deficiency

Plantar fibromatosis

Left ventricular hypertrophy

Legg–Calvé–Perthes syndrome

Legionnaires' disease

Leigh's disease

Leiner's disease

Lemierre's syndrome

Lennox–Gastaut syndrome

Lenz microphthalmia syndrome

Donohue syndrome

Leri pleonosteosis

Léri–Weill dyschondrosteosis

Lethal congenital contracture syndrome

Letterer–Siwe disease

Maple syrup urine disease

Myeloid leukemia

T-cell prolymphocytic leukemia

Leukocyte adhesion deficiency

Periventricular leukomalacia

Neuroacanthocytosis

Leaky gut syndrome

Lhermitte–Duclos disease

Lichen myxedematosus

Lichen sclerosus

Lichen spinulosus

Liddle's syndrome

Li–Fraumeni syndrome

Light chain deposition disease

Limb-girdle muscular dystrophy

Urbach–Wiethe disease

Livedoid dermatitis

Locked-in syndrome

Loa loa filariasis

Loin pain hematuria syndrome

Long QT syndrome

Loose anagen syndrome

Oculocerebrorenal syndrome

Lowry–MacLean syndrome

Levo-Transposition of the great arteries

Lucey–Driscoll syndrome

Problem gambling

Lujan–Fryns syndrome

Lumbar spinal stenosis

Lupus anticoagulant

Toxic epidermal necrolysis

Lymphangiectasia

Lymphangioleiomyomatosis

Lymphatic filariasis

Lymphedema–distichiasis syndrome

Milroy's disease

Congenital lymphedema

Lymphoblastic lymphoma

Lymphocytic colitis

Cutaneous lymphoid hyperplasia

AIDS-related lymphoma

Small cleaved cells

Lymphomatoid papulosis

Lyngstadaas syndrome

Lysosomal storage disease

Macroglobulinemia

Beckwith–Wiedemann syndrome

Macrophagic myofasciitis

May–Hegglin anomaly

Macular corneal dystrophy

Vitelliform macular dystrophy

Bovine spongiform encephalopathy

Benign symmetric lipomatosis

Maffucci syndrome

Mal de debarquement

Pleomorphic undifferentiated sarcoma

Mallory–Weiss syndrome

Malonyl-CoA decarboxylase deficiency

Malouf syndrome

Malpuech facial clefting syndrome

Mandibuloacral dysplasia

Mantle cell lymphoma

Marburg virus disease

Marchiafava–Bignami disease

Marcus Gunn phenomenon

Marden–Walker syndrome

Marek's disease

Marfan syndrome

Loeys–Dietz syndrome

Marinesco–Sjögren syndrome

Maroteaux–Lamy syndrome

Marshall–Smith syndrome

Mass psychogenic illness

Hypermethioninemia

Diabetes mellitus and deafness

Maturity onset diabetes of the young

Binder's syndrome

Müllerian agenesis

McGillivray syndrome

McKusick–Kaufman syndrome

Meadow's syndrome

Medullary cystic kidney disease

Medullary thyroid cancer

Medulloblastoma

Otospondylomegaepiphyseal dysplasia

Megaloblastic anemia

Meige's syndrome

Melkersson–Rosenthal syndrome

Melnick–Needles syndrome

Ménétrier's disease

Ménière's disease

Meningococcal disease

Intellectual disability

Mercury poisoning

Ardalan–Shoja–Kiuru syndrome

Mesenteric ischemia

Metabolic acidosis

Metabolic syndrome

Metachondromatosis

Methylmalonic acidemia

Methylmalonyl-CoA mutase deficiency

Mevalonate kinase deficiency

Relapsing polychondritis

Michelin tire baby syndrome

Michels syndrome

Mickleson syndrome

Microcephaly lymphoedema chorioretinal dysplasia

Macular hypoplasia

Microscopic polyangiitis

Microsporidiosis

Sjögren's syndrome

Microphthalmia–dermal aplasia–sclerocornea syndrome

Benign lymphoepithelial lesion

Mild cognitive impairment

Miller–Dieker syndrome

Minamata disease

Mirhosseini–Holmes–Walton syndrome

Mitochondrial disease

Mitochondrial trifunctional protein deficiency

Mitral valve prolapse

Mixed connective tissue disease

Mixed Müllerian tumor

Mixed receptive-expressive language disorder

Orofaciodigital syndrome 1

Mohr–Tranebjærg syndrome

Molluscum contagiosum

Molybdenum cofactor deficiency

Mondini dysplasia

Mondor's disease

Brunner syndrome

Monoclonal gammopathy of undetermined significance

Motor neuron disease

Tracheobronchomegaly

Moyamoya disease

Myeloperoxidase deficiency

Sanfilippo syndrome

Pityriasis lichenoides et varioliformis acuta

Muckle–Wells syndrome

Hereditary mucoepithelial dysplasia

Pseudo-Hurler polydystrophy

Mucolipidosis type IV

Mucopolysaccharidosis

Multiple sulfatase deficiency

Muenke syndrome

Mulibrey nanism

Multicentric reticulohistiocytosis

Multifocal motor neuropathy

Premature ventricular contraction

Multiple chemical sensitivity

Multiple endocrine neoplasia type 1

Multiple endocrine neoplasia type 2

Multiple myeloma

Multiple organ dysfunction syndrome

Multiple sclerosis

Multiple system atrophy

Münchausen syndrome

Münchausen syndrome by proxy

Myasthenia gravis

Mycobacterium avium-intracellulare infection

Atypical pneumonia

Mycosis fungoides

Myelodysplastic syndrome

Myoclonic dystonia

Myoclonic epilepsy

Unverricht–Lundborg disease

Myopathy, X-linked, with excessive autophagy

Myositis ossificans

Inclusion body myositis

Myxoid liposarcoma

N-Acetylglutamate synthase deficiency

Naegeli–Franceschetti–Jadassohn syndrome

Nail–patella syndrome

Nakajo syndrome

Nance–Horan syndrome

Narcissistic personality disorder

Nasodigitoacoustic syndrome

Nasopharynx cancer

Neisseria meningitidis

Nelson's syndrome

Nemaline myopathy

Neonatal diabetes mellitus

Permanent neonatal diabetes mellitus

Transient neonatal diabetes mellitus

Neonatal hemochromatosis

Neonatal hepatitis

Neonatal jaundice

Large for gestational age

Nephrocalcinosis

Nephronophthisis

Hypertensive nephropathy

Nephrotic syndrome

Nerve sheath tumor

Nesidioblastosis

Neural tube defect

Galactosialidosis

Infantile neuroaxonal dystrophy

Neurocutaneous melanosis

Neurofibrillary tangle

Neurofibromatosis

Neurofibromatosis type 3

Neurofibromatosis type 4

Watson syndrome

Malignant peripheral nerve sheath tumor

Neuroleptic malignant syndrome

Nevoid basal cell carcinoma syndrome

Nezelof syndrome

Nicolaides–Baraitser syndrome

Nicotine withdrawal

Niemann–Pick disease

Niemann–Pick disease, type C

X-linked congenital stationary night blindness

Olney's lesions

Noise-induced hearing loss

Non-24-hour sleep–wake disorder

Non-Hodgkin lymphoma

Glycine encephalopathy

Non-small-cell lung carcinoma

Nonverbal learning disorder

Noonan syndrome

Norman–Roberts syndrome

Northern epilepsy syndrome

Notalgia paresthetica

Tree nut allergy

Zonular cataract and nystagmus

Obsessive–compulsive disorder

Obsessive–compulsive personality disorder

Obstructive sleep apnea

Occipital horn syndrome

Occupational asthma

Urofacial syndrome

Pogosta disease

Ocular albinism

Presumed ocular histoplasmosis syndrome

Toxoplasmic chorioretinitis

Oculodentodigital dysplasia

Oculocutaneous albinism type I

Oculomotor nerve palsy

Oculopharyngeal muscular dystrophy

Ogilvie syndrome

Oliver–McFarlane syndrome

Olivopontocerebellar atrophy

Palmoplantar keratoderma

Omsk hemorrhagic fever

Onychogryphosis

Onychomatricoma

Opioid dependence

Opioid-induced hyperalgesia

Opportunistic infection

Oppositional defiant disorder

Opsismodysplasia

Optic disc drusen

Optic nerve hypoplasia

Sugarman syndrome

Oral submucous fibrosis

Organic brain syndrome

Organophosphate poisoning

Ornithine aminotransferase deficiency

Orotic aciduria

Orthostatic intolerance

Osgood–Schlatter disease

Paget's disease of bone

Osteochondritis dissecans

Osteochondritis

Avascular necrosis

Osteopoikilosis

Otodental syndrome

Overwhelming post-splenectomy infection

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