FACTOID # 177: 61.5% of Swedes work more than 40 hours per week, but just across the border in Norway only 15.8% of people work this long.
 
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Encyclopedia > List of diseases starting with O

A list of diseases in the English wikipedia. A disease is any abnormal condition of the body or mind that causes discomfort, dysfunction, or distress to the person affected or those in contact with the person. ...


A B C D E F G H I J K L M N O P Q R S T U V W X Y Z A listing of diseases. ... A listing of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ...

Contents


O-Ob

Oc

Occ-Och

  • Occipital horn syndrome
  • Occlusive Infantile ateriopathy
  • Occult spinal dysraphism
  • Occupational Asthma - Chemicals
  • Occupational Asthma - Metals
  • Occupational Asthma - Plants
  • Occupational Asthma - Wood dust
  • Occupational Asthma-Drugs
  • OCD
  • Ochoa syndrome
  • Ochronosis, hereditary
  • Ochronosis

Occipital horn syndrome is a variant of Ehlers Danlos syndrome. ... For other things named OCD, see OCD (disambiguation). ...

Ocu

Ocul

Ocula
  • Ocular Albinism
  • Ocular coloboma-imperforate anus
  • Ocular convergence spasm
  • Ocular Histoplasmosis
  • Ocular melanoma
  • Ocular motility disorders
  • Ocular toxoplasmosis

Oculo
  • Oculo cerebral dysplasia
  • Oculo cerebro acral syndrome
  • Oculo cerebro osseous syndrome
  • Oculo dento digital dysplasia
  • Oculo digital syndrome
  • Oculo facio cardio dental syndrome
  • Oculo skeletal renal syndrome
  • Oculo tricho anal syndrome
  • Oculo tricho dysplasia

Oculoa-Oculog
  • Oculoauriculofrontonasal syndrome
  • Oculoauriculovertebral dysplasia
  • Oculocerebral hypopigmentation syndrome Cross type
  • Oculocerebral hypopigmentation syndrome type Preus
  • Oculocerebral syndrome with hypopigmentation
  • Oculocerebrocutaneous syndrome
  • Oculocerebrorenal syndrome
  • Oculocutaneous albinism immunodeficiency
  • Oculocutaneous albinism type 1
  • Oculocutaneous albinism type 2
  • Oculocutaneous albinism type 3
  • Oculocutaneous albinism, tyrosinase negative
  • Oculocutaneous albinism, tyrosinase positive
  • Oculocutaneous tyrosinemia
  • Oculodental syndrome Rutherfurd syndrome
  • Oculodentodigital dysplasia dominant
  • Oculodentodigital syndrome
  • Oculo-dento-digital syndrome
  • Oculodentoosseous dysplasia dominant
  • Oculodentoosseous dysplasia recessive
  • Oculodigitoesophagoduodenal syndrome
  • Oculo-gastrointestinal muscular dystrophy

Albinism is a genetic condition resulting in a lack of pigmentation in the eyes, skin and hair. ...

Oculom-Oculor
  • Oculomaxillofacial dysostosis
  • Oculomaxillofacial dysplasia with oblique facial clefts
  • Oculomelic amyoplasia
  • Oculopalatoskeletal syndrome
  • Oculopharyngeal muscular dystrophy
  • Oculorenocerebellar syndrome

Oculopharyngeal dystrophy (OPD), or oculopharyngeal muscular dystrophy, is a form of muscular dystrophy characterized in some stages by deformation of the eyelid, speech impediment, and difficulty swallowing due to dystrophia of the pharynx. ...

Od-Ok

  • Odonto onycho dysplasia with alopecia
  • Odontoma
  • Odontomicronychial dysplasia
  • Odontoonychodermal dysplasia
  • Odontophobia
  • Odontotrichomelic hypohidrotic dysplasia
  • Odynophobia
  • OFD syndrome type 8
  • OFD syndrome type Figuera
  • Ogilvie's syndrome
  • Ohaha syndrome
  • Ohdo Madokoro Sonoda syndrome
  • Oikophobia
  • Okamuto Satomura syndrome

The English suffix -phobia is used to describe fear or hatred (the latter is often ignored) of a particular thing or subject. ... The English suffix -phobia is used to describe fear or hatred (the latter is often ignored) of a particular thing or subject. ...

Ol

  • Olfactophobia
  • Oligodactyly tetramelic postaxial
  • Oligomeganephronic renal hypoplasia
  • Oligomeganephrony
  • Oligophernia
  • Oliver McFarlane syndrome
  • Oliver syndrome
  • Olivopontocerebellar atrophy deafness
  • Olivopontocerebellar atrophy type 1
  • Olivopontocerebellar atrophy type 2
  • Olivopontocerebellar atrophy type 3
  • Olivopontocerebellar atrophy
  • Ollier disease
  • Olmsted syndrome

The English suffix -phobia is used to describe fear or hatred (the latter is often ignored) of a particular thing or subject. ... These are a group of diseases characterized by neuronal degeneration in the cerebellum, pontine nuclei, and inferior olive. ...

Om-On

  • Ombrophobia
  • Omenn syndrome
  • Omodysplasia type 1
  • Omphalocele cleft palate syndrome lethal
  • Omphalocele exstrophy imperforate anus
  • Omphalomesenteric cyst
  • Omsk hemorrhagic fever
  • Onat syndrome
  • Onchocerciasis
  • Oncocytoma
  • Ondine's curse
  • Oneirophobia
  • Onychonychia hypoplastic distal phalanges
  • Onychotrichodysplasia and neutropenia

Onchocerciasis or river blindness is the worlds second leading infectious cause of blindness. ... Ondines curse, or central alveolar hypoventilation syndrome, is a respiratory disorder that is fatal if untreated. ...

Op

Oph

  • Ophthalmic icthyosis
  • Ophthalmo acromelic syndrome
  • Ophthalmomandibulomelic dysplasia
  • Ophthalmophobia
  • Ophthalmoplegia ataxia hypoacusis
  • Ophthalmoplegia mental retardation lingua scrotalis
  • Ophthalmoplegia myalgia tubular aggregates
  • Opitz Mollica Sorge syndrome
  • Opitz Reynolds Fitzgerald syndrome
  • Opitz syndrome
  • Opportunistic infections
  • Oppositional defiant disorder
  • Opsismodysplasia

Opportunistic infections are infections in immunodeficient patients caused by pathogens which are incapable of causing infection in immunocompetent individuals. ...

Opt

  • Opthalmoplegia progressive external scoliosis
  • Optic atrophy opthalmoplegia ptosis deafness myopia
  • Optic atrophy polyneuropathy deafness
  • Optic atrophy, autosomal dominant
  • Optic atrophy, idiopathic, autosomal recessive
  • Optic atrophy
  • Optic nerve coloboma with renal disease
  • Optic nerve disorder
  • Optic nerve hypoplasia, familial bilateral
  • Optic neuritis
  • Optic pathway glioma
  • Opticoacoustic nerve atrophy dementia

Optic atrophy is a general term for a dysfunction of the optic nerve. ... Optic neuritis is the inflammation of the optic nerve that may cause a complete or partial loss of vision. ...

Or

Ora-Orn

  • Oral facial digital syndrome type 3
  • Oral facial digital syndrome type 4
  • Oral facial digital syndrome
  • Oral facial dyskinesia
  • Oral leukoplakia
  • Oral lichen planus
  • Oral lichenoid lesions
  • Oral squamous cell carcinoma
  • Oral submucous fibrosis
  • Oral-facial cleft
  • Oral-facial-digital syndrome, type IV
  • Oral-facial-digital syndrome
  • Oral-pharyngeal disorders
  • Organic brain syndrome
  • Organic mood syndrome
  • Organic personality syndrome
  • Ornithine aminotransferase deficiency
  • Ornithine carbamoyl phosphate deficiency
  • Ornithine transcarbamylase deficiency, hyperammonemia due to
  • Ornithinemia

Oro-Ort

  • Oro acral syndrome
  • Orofaciodigital syndrome Gabrielli type
  • Orofaciodigital syndrome Shashi type
  • Orofaciodigital syndrome Thurston type
  • Orofaciodigital syndrome type 2
  • Orofaciodigital syndrome type1
  • Orotic aciduria hereditary
  • Orotic aciduria purines-pyrimidines
  • Orotidylic decarboxylase deficiency
  • Orstavik Lindemann Solberg syndrome
  • Orthostatic intolerance

Orthostatic intolerance is the failure of the body to properly adjust to an upright position, especially with respect to blood flow, heart rate, and blood pressure. ...

Os

Ose-Oss

  • Osebold Remondini syndrome
  • Oslam syndrome
  • Osmed Syndrome
  • Ossicular Malformations, familial

Ost

Oste

Ostei

Osteo

osteo: bone Grays illustration of a human femur, a typically recognized bone. ...


Osteoa-Osteom
  • Osteoarthritis
  • Osteoarthropathy of fingers familial
  • Osteochondritis deformans juvenile
  • Osteochondritis dissecans
  • Osteochondritis
  • Osteochondrodysplasia thrombocytopenia hydrocephalus
  • Osteochondroma
  • Osteocraniostenosis
  • Osteodysplasia familial Anderson type
  • Osteodysplastic dwarfism Corsello type
  • Osteoectasia familial
  • Osteogenesis Imperfecta
  • Osteogenesis imperfecta congenita microcephaly and cataracts
  • Osteogenesis imperfecta congenital joint contractures
  • Osteogenesis imperfecta retinopathy
  • Osteogenic sarcoma
  • Osteoglophonic dwarfism
  • Osteolysis hereditary multicentric
  • Osteolysis syndrome recessive
  • Osteomalacia
  • osteomyelitis

Osteoarthritis (OA), also known as arthrosis or degenerative joint disease, is a disease featuring pain and impaired function of the joints. ... Osteogenesis imperfecta (OI), commonly known as brittle bone disease, is a group of genetic bone disorders. ...

Osteon-Osteos
  • Osteonecrosis
  • Osteopathia condensans disseminata with osteopoikilosis
  • Osteopathia striata cranial sclerosis
  • Osteopathia striata pigmentary dermopathy white forelock
  • Osteopetrosis autosomal dominant type 1
  • Osteopetrosis lethal
  • Osteopetrosis renal tubular acidosis
  • Osteopetrosis, (generic term)
  • Osteopetrosis, malignant
  • Osteopetrosis, mild autosomal recessive form
  • Osteopoikilosis
  • Osteoporosis macrocephaly mental retardation blindness
  • Osteoporosis oculocutaneous hypopigmentation syndrome
  • Osteoporosis pseudoglioma syndrome
  • osteoporosis
  • Osteosarcoma limb anomalies erythroid macrocytosis
  • Osteosclerose type Stanescu
  • Osteosclerosis abnormalities of nervous system and meninges
  • Osteosclerosis autosomal dominant Worth type
  • Osteosclerosis

Osteoporosis is a disease of bone in which the amount of bone is decreased and the strength of trabecular bone is reduced, cortical bone becomes thin and bones are susceptible to fracture. ...

Oster
  • Ostertag type amyloidosis

Ot-Ox

  • Ota Kawamura Ito syndrome
  • Oto palato digital syndrome type I and II
  • Otodental dysplasia
  • Otofaciocervical syndrome
  • Otoonychoperoneal syndrome
  • Oto-Palatal-digital syndrome
  • Otopalatodigital syndrome type 2
  • Otosclerosis, familial
  • otosclerosis
  • Otospondylomegaepiphyseal dysplasia
  • Ouvrier Billson syndrome
  • Ovarian cancer
  • Ovarian carcinosarcoma
  • Ovarian dwarfism as part of Turner Syndrome
  • Ovarian dwarfism
  • Ovarian insufficiency due to FSH resistance
  • ovarian remnant syndrome
  • Overfolded helix
  • Overgrowth radial ray defect arthrogryposis
  • Overgrowth syndrome type Fryer
  • Overhydrated hereditary stomatocytosis
  • Oxalosis


 

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