List of diseases (O)
This is a list of diseases starting with the letter "O".
O–Ob
Oc
Occ–Och
- Occipital horn syndrome
- Occlusive infantile arteriopathy
- Occult spinal dysraphism
- Occupational asthma
- Occupational asthma - animals, insects and fungi
- Occupational asthma - chemicals and materials
- Occupational asthma - drugs and enzymes
- Occupational asthma - grains, flours, plants and gums
- Occupational asthma - isocyanates and metals
- Occupational asthma - wood
- OCD
- Ochoa syndrome
- Ochronosis, hereditary
- Ochronosis
- Ockelbo disease
Ocu
Ocul
Ocula
Oculo
- Oculo-auriculo-vertebral spectrum
- Oculo cerebral dysplasia
- Oculo-cerebro-acral syndrome[3]
- Oculo-cerebro-renal syndrome[4]
- Oculodentodigital dysplasia[5][6]
- Oculofaciocardiodental syndrome[7]
Oculoa–Oculog
- Oculoauriculofrontonasal syndrome
- Oculo-auriculo-vertebral dysplasia
- Oculocerebral hypopigmentation syndrome Cross type[8]
- Oculocerebral hypopigmentation syndrome (Preus type)[9]
- 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
- Oculodentodigital dysplasia dominant
- Oculodentodigital syndrome
- Oculo-dento-digital syndrome
- Oculodentoosseous dysplasia dominant
- Oculodentoosseous dysplasia recessive
- Oculodigitoesophagoduodenal syndrome
- Oculogastrointestinal muscular dystrophy[10]
Oculom–Oculor
- Oculomaxillofacial dysostosis[11]
- Oculomaxillofacial dysplasia[11]
- Oculomelic amyoplasia
- Oculomotor nerve palsy
- Oculopalatoskeletal syndrome
- Oculopharyngeal muscular dystrophy
Od–Ok
- Odonto onycho dysplasia with alopecia
- Odontoma
- Odontomicronychial dysplasia
- Odontoonychodermal dysplasia
- Odontophobia
- Odontotrichomelic hypohidrotic dysplasia
- OFD syndrome type 8
- OFD syndrome type Figuera
- Ogilvie's syndrome
- Ohaha syndrome
- Ohdo–Madokoro–Sonoda syndrome
- Oikophobia
- Okamuto–Satomura syndrome
Ol
- Olfactophobia
- Oligodactyly
- Oligodactyly tetramelia 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
- Olney's lesions
Om–On
- Omenn syndrome
- Omodysplasia type 1
- Omodysplasia type 2
- Omphalocele cleft palate syndrome lethal
- Omphalocele exstrophy imperforate anus
- Omphalomesenteric cyst
- Omsk hemorrhagic fever
- Onat syndrome
- Onchocerciasis
- Oncocytoma
- Ondine's curse
- Oneirophobia
- Onychocryptosis
- Onychogryphosis
- Onycholysis
- Onychomadesis
- Onychomatricoma
- Onychomycosis
- Onychonychia hypoplastic distal phalanges
- Onychophosis
- Onychotrichodysplasia and neutropenia
Op
Opi-Ops
- Opioid dependence
- Opioid-induced hyperalgesia
- Ophthalmic icthyosis
- Ophthalmo acromelic syndrome
- Ophthalmomandibulomelic dysplasia
- Ophthalmophobia
- Ophthalmoplegia ataxia hypoacusis
- Ophthalmoplegia mental retardation lingua scrotalis
- Ophthalmoplegia myalgia tubular aggregates
- Ophthalmoplegia progressive external scoliosis
- Opitz–Mollica–Sorge syndrome
- Opitz–Reynolds–Fitzgerald syndrome
- Opitz syndrome
- Opportunistic infections
- Oppositional defiant disorder
- Opsismodysplasia
Opt
- Optic atrophy ophthalmoplegia ptosis deafness myopia
- Optic atrophy polyneuropathy deafness
- Optic atrophy, autosomal dominant
- Optic atrophy, idiopathic, autosomal recessive
- Optic atrophy
- Optic disc drusen
- Optic nerve coloboma with renal disease
- Optic nerve disorder
- Optic nerve hypoplasia, familial bilateral
- Optic neuritis
- Optic pathway glioma
- Opticoacoustic nerve atrophy dementia
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
- Organophosphate poisoning
- Ornithine aminotransferase deficiency
- Ornithine carbamoyl phosphate deficiency
- Ornithine transcarbamylase deficiency, hyperammonemia due to
- Ornithinemia
- Ornithosis
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
Os
Ose–Oss
- Osebold–Remondini syndrome
- Osgood–Schlatter disease
- OSLAM syndrome
- Osmed syndrome
- Ossicular malformations, familial
Ost
Oste
Ostei
Osteo
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
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
- Osteocytes
Oster
Ot–Ox
- Ota–Appaura syndrome
- Ota–Kawamura–Ito syndrome
- Oto-palato-digital syndrome type I and II
- Otodental syndrome
- 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
- Overwhelming post-splenectomy infection (OPSI)
- Oxalosis
References
- ↑ Sharma, S.; Gupta, N.; Gupta, P.; Goutam, T. (2024). "Obesity, pocresophobia and oral health". Przeglad Epidemiologiczny. 78 (2): 177–181. doi:10.32394/pe/188703.
- ↑ Sandri, E.; Cantín Larumbe, E.; Cerdá Olmedo, G.; Luciani, G.; Mancin, S.; Sguanci, M.; Piredda, M. (2024). "Anorexia and Bulimia Nervosa in Spanish Middle-Aged Adults: Links to Sociodemographic Factors, Diet, and Lifestyle". Nutrients. 16 2671. doi:10.3390/nu16162671.
{{cite journal}}: CS1 maint: unflagged free DOI (link) - ↑ Atkin, J.F.; Patil, S. (1984). "Apparently new oculo-cerebro-acral syndrome". American Journal of Medical Genetics. 19 (3): 585–587. doi:10.1002/ajmg.1320190322.
- ↑ Richards, W.; Donnell, G.N.; Wilson, W.A.; Stowens, D.; Perry, T. (1965). "The Oculo-Cerebro-Renal Syndrome of Lowe". Journal of the American Medical Association, Pediatrics. 109 (3): 185–203. doi:10.1001/archpedi.1965.02090020187001.
- ↑ Loddenkemper, T.; Grote, K.; Evers, S.; Oelerich, M.; Stögbauer, F. (2002). "Neurological manifestations of the oculodentodigital dysplasia syndrome". Journal of Neurology. 249: 584–595. doi:10.1007/s004150200068.
- ↑ Judisch, G.F.; Martin-Casals, A.; Hanson, J.W.; Olin, W.H. (1979). "Oculodentodigital Dysplasia: Four New Reports and a Literature Review". Journal of the American Medical Association - Ophthalmology. 97 (5): 878–884. doi:10.1001/archopht.1979.01020010436007.
- ↑ Davoody, A.; Chen, I.-P.; Nanda, R.; Uribe, F.; Reichenberger, E.J. (2012). "Oculofaciocardiodental Syndrome: A Rare Case and Review of the Literature". The Cleft Palate Craniofacial Journal. 49 (5): 55–60. doi:10.1597/10-256.
- ↑ Cross, H.E.; McKusick, V.A.; Breen, W. (1967). "A new oculocerebral syndrome with hypopigmentation". Journal of Pediatrics. 70 (3): 398–406. doi:10.1016/S0022-3476(67)80137-9. PMID 4959856.
- ↑ Preus, M.; Fraser, F.C.; Wiglesworth, F.W. (1983). "An oculocerebral hypopigmentation syndrome". Journal de Genetique Humaine. 31 (4): 323–328. PMID 6663291.
- ↑ Ionasescu, Victor (1983). "Oculogastrointestinal Muscular Dystrophy". American Journal of Medical Genetics. 15: 103–112. doi:10.1002/ajmg.1320150114.
- 1 2 Richieri-Costa, A.; Gorlin, R.J. (1994). "Oblique Facial Clefts: Report on 4 Brazilian Patients. Evidence for Clinical Variability and Genetic Heterogeneity". American Journal of Medical Genetics. 53: 222–226. doi:10.1002/ajmg.1320530305.
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