List of diseases (O)
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Diseases |
O-Ob
- O Doherty syndrome
- O Donnell Pappas syndrome
- Obesity
- Obesophobia
- Obsessive-compulsive disorder
- Obstructive asymmetric septal hypertrophy
- Obstructive sleep apnea
Oc
Occ-Och
- Occipital horn syndrome
- Occlusive Infantile ateriopathy
- Occult spinal dysraphism
- Occupational asthma
- Occupational asthma - Chemicals
- Occupational asthma - Metals
- Occupational asthma - Plants
- Occupational asthma - Wood dust
- Occupational asthma - Drugs
- OCD
- Ochoa syndrome
- Ochronosis, hereditary
- Ochronosis
- Ockelbo disease
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
Oculom-Oculor
- Oculomaxillofacial dysostosis
- Oculomaxillofacial dysplasia with oblique facial clefts
- Oculomelic amyoplasia
- Oculopalatoskeletal syndrome
- Oculopharyngeal muscular dystrophy
- Oculorenocerebellar syndrome
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
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
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
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
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
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
- 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
Oster
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
- Overwhelming post-splenectomy infection (OPSI)
- Oxalosis
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
