List of rare diseases starting with O
This list of rare diseases was originally taken from the NIH public domain resource at http://ord.aspensys.com/asp/diseases/diseases.asp .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
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2 Oe-Oh 3 Oi-Ol 4 Om-Op 5 Oq-Ot 6 Ou-Oz |
Oa-Od
- O Doherty syndrome
- O Donnell Pappas syndrome
- Obesity
- Obesophobia
- Obsessive-compulsive disorder
- Obstructive asymmetric septal hypertrophy
- 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
- Ocular Albinism
- Ocular coloboma-imperforate anus
- Ocular convergence spasm
- Ocular Histoplasmosis
- Ocular melanoma
- Ocular motility disorders
- Ocular toxoplasmosis
- 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
- 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
- Oculomaxillofacial dysostosis
- Oculomaxillofacial dysplasia with oblique facial clefts
- Oculomelic amyoplasia
- Oculopalatoskeletal syndrome
- Oculopharnygeal muscular dystrophy
- Oculorenocerebellar syndrome
- Odonto onycho dysplasia with alopecia
- Odontoma
- Odontomicronychial dysplasia
- Odontoonychodermal dysplasia
- Odontophobia
- Odontotrichomelic hypohidrotic dysplasia
- Odynophobia
Oe-Oh
- OFD syndrome type 8
- OFD syndrome type Figuera
- Ogilvie's syndrome
- Ohaha syndrome
- Ohdo Madokoro Sonoda syndrome
Oi-Ol
- Oikophobia
- Okamuto Satomura syndrome
- 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
Om-Op
- 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
- Ophthalmophobia
- Opitz Mollica Sorge syndrome
- Opitz Reynolds Fitzgerald syndrome
- Opitz syndrome
- Opportunistic infections
- Oppositional defiant disorder
- Opsismodysplasia
- Ophthalmic icthyosis
- Ophthalmo acromelic syndrome
- Ophthalmomandibulomelic dysplasia
- Ophthalmoplegia ataxia hypoacusis
- Ophthalmoplegia mental retardation lingua scrotalis
- Ophthalmoplegia myalgia tubular aggregates
- 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
Oq-Ot
- 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 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
- Oslam syndrome
- Osmed Syndrome
- Ossicular Malformations, familial
- Osteitis deformans
- 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 congenita microcephaly and cataracts
- Osteogenesis imperfecta congenital joint contractures
- Osteogenesis imperfecta retinopathy
- Osteogenic sarcoma
- Osteoglophonic dwarfism
- Osteolysis hereditary multicentric
- Osteolysis syndrome recessive
- Osteomalacia
- osteomyelitis
- 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
- Ostertag type amyloidosis
- 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
Ou-Oz
- 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
