List of diseases (O)

• Occipital horn syndrome
• Occlusive Infantile ateriopathy
• 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

• Ocular albinism
• Ocular coloboma-imperforate anus
• Ocular convergence spasm
• Ocular histoplasmosis
• Ocular melanoma
• Ocular motility disorders
• Ocular toxoplasmosis

• Oculo-auriculo-vertebral spectrum
• 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

• Oculoauriculofrontonasal syndrome
• Oculo-auriculo-vertebral 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

• Oculomaxillofacial dysostosis
• Oculomaxillofacial dysplasia with oblique facial clefts
• Oculomelic amyoplasia
• Oculomotor nerve palsy
• Oculopalatoskeletal syndrome
• Oculopharyngeal muscular dystrophy
• Oculorenocerebellar syndrome

• 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

• 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

• 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 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

• Osebold–Remondini syndrome
• Osgood–Schlatter disease
• OSLAM syndrome
• Osmed syndrome
• Ossicular malformations, familial

• Osteitis deformans

osteo: bone

• 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

osteocytes

• 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

• Ostertag type amyloidosis