FANDOM


OA-1 [↗]
OAV dysplasia [↗]
OAV spectrum [↗]
Oberklaid-Danks syndrome [↗]
Obesity - colitis - hypothyroidism - cardiac hypertrophy - developmental delay [↗]
Obesity due MC3R deficiency [↗]
Obesity due to congenital leptin deficiency [↗]
Obesity due to leptin receptor gene deficiency [↗]
Obesity due to melanocortin-4 receptor deficiency [↗]
Obesity due to prohormone convertase-I deficiency [↗]
Obesity due to pro-opiomelanocortin deficiency [↗]
Obliterative portal venopathy [↗]
OCA [↗]
OCA-1A [↗]
OCA-1B [↗]
OCA-2 [↗]
OCA-3 [↗]
OCA-4 [↗]
Occipital atretic cephalocele - unusual facies - large feet [↗]
Occipital encephalocele [↗]
Occipital horn syndrome [↗]
Occipital malformations of cortical development [↗]
Occipital MCD [↗]
Occipital pachygyria and polymicrogyria [↗]
Occlusive infantile arteriopathy [↗]
OCCS [↗]
Occult macular dystrophy [↗]
Occult spinal dysraphism [↗]
Occupational allergic alveolitis [↗]
Ochoa syndrome [↗]
OCR [↗]
OCRL [↗]
OCT deficiency [↗]
Ocular albinism - late-onset sensorineural deafness [↗]
Ocular albinism, Nettleship-Falls type [↗]
Ocular albinism type 1 [↗]
Ocular coloboma - imperforate anus [↗]
Ocular form of osteogenesis imperfecta [↗]
Ocular motor apraxia, Cogan type [↗]
Ocular pemphigoid [↗]
Oculoauricular syndrome, Schorderet type [↗]
Oculo-auriculo-fronto-nasal syndrome [↗]
Oculoauriculovertebral dysplasia [↗]
Oculo-auriculo-vertebral spectrum [↗]
Oculoauriculovertebral spectrum with radial defects [↗]
Oculocerebral dysplasia [↗]
Oculocerebral hypopigmentation syndrome, Cross type [↗]
Oculocerebral hypopigmentation syndrome, Preus type [↗]
Oculo-cerebro-acral syndrome [↗]
Oculocerebrocutaneous syndrome [↗]
Oculocerebrofacial syndrome, Kaufman type [↗]
Oculo-cerebro-osseous syndrome [↗]
Oculocerebrorenal dystrophy [↗]
Oculo-cerebro-renal dystrophy [↗]
Oculocerebrorenal syndrome [↗]
Oculo-cerebro-renal syndrome [↗]
Oculocutaneous albinism [↗]
Oculocutaneous albinism type 1A [↗]
Oculocutaneous albinism type 1B [↗]
Oculocutaneous albinism type 2 [↗]
Oculocutaneous albinism type 3 [↗]
Oculocutaneous albinism type 4 [↗]
Oculocutaneous albinism type Amish [↗]
Oculocutaneous tyrosinemia [↗]
Oculodental syndrome, Rutherfurd type [↗]
Oculodentodigital dysplasia [↗]
Oculodentoosseous dysplasia [↗]
Oculo digital syndrome [↗]
Oculo-digito-esophageal-duodenal syndrome [↗]
Oculoectodermal syndrome [↗]
Oculofaciocardiodental syndrome [↗]
Oculogastrointestinal muscular dystrophy [↗]
Oculomaxillofacial dysostosis [↗]
Oculomelic amyoplasia [↗]
Oculoosteocutaneous syndrome [↗]
Oculootodental syndrome [↗]
Oculo-oto-facial dysplasia [↗]
Oculo-oto-radial syndrome [↗]
Oculo-palato-cerebral dwarfism [↗]
Oculo-palato-cerebral syndrome [↗]
Oculopalatoskeletal syndrome [↗]
Oculopharyngeal muscular dystrophy [↗]
Oculopharyngodistal myopathy [↗]
Oculo-reno-cerebellar syndrome [↗]
Oculo-skeletal-abdominal syndrome [↗]
Oculo-skeletal-renal syndrome [↗]
Oculotrichoanal syndrome [↗]
Oculotrichodysplasia [↗]
ODDD syndrome [↗]
ODED syndrome [↗]
O'Doherty syndrome [↗]
O Donnell-Pappas syndrome [↗]
Odontochondrodysplasia [↗]
Odontohypophosphatasia [↗]
Odontoleukodystrophy [↗]
Odontomatosis - aortae esophagus stenosis [↗]
Odontomicronychial dysplasia [↗]
Odonto-onycho-dermal dysplasia [↗]
Odonto-onycho dysplasia - alopecia [↗]
Odontotrichomelic syndrome [↗]
Odonto-tricho-ungual-digito-palmar syndrome [↗]
Odonto-tricho-ungual-digito-palmar syndrome, Mendoza-Valiente type [↗]
ODP [↗]
OEIS complex [↗]
Oerter-Friedman-Anderson syndrome [↗]
OFCD syndrome [↗]
OFC syndrome [↗]
OFD1 [↗]
OFD10 [↗]
OFD11 [↗]
OFD2 [↗]
OFD3 [↗]
OFD4 [↗]
OFD5 [↗]
OFD6 [↗]
OFD7 [↗]
OFD8 [↗]
OFD9 [↗]
Oguchi disease [↗]
Oguchi's disease [↗]
Oguchi's syndrome [↗]
Ohaha syndrome [↗]
Ohdo blepharophimosis syndrome [↗]
Ohdo-Madokoro-Sonoda syndrome [↗]
Ohdo syndrome [↗]
OHSS [↗]
Ohtahara syndrome [↗]
OI [↗]
OI type 1 [↗]
OI type 2 [↗]
OI type 3 [↗]
OI type 4 [↗]
OI type 5 [↗]
Okamoto syndrome [↗]
Okihiro syndrome [↗]
Okihiro syndrome due to 20q13 microdeletion [↗]
Okihiro syndrome due to a point mutation [↗]
Okihiro syndrome due to del(20)(q13) [↗]
Okihiro syndrome due to monosomy 20q13 [↗]
OL-EDA-ID [↗]
Olfactory neuroblastoma [↗]
Oligoarticular juvenile arthritis [↗]
Oligoarticular juvenile arthritis with anti-nuclear antibodies [↗]
Oligoarticular juvenile arthritis without anti-nuclear antibodies [↗]
Oligoastrocytoma [↗]
Oligocone syndrome [↗]
Oligocone trichromacy [↗]
Oligodendroglial tumor [↗]
Oligodendroglioma [↗]
Oligodontia [↗]
Oligomeganephronia [↗]
Oligomeganephronic renal hypoplasia [↗]
Oliver-McFarlane syndrome [↗]
Oliver syndrome [↗]
Olivopontocerebellar atrophy - deafness [↗]
Ollier disease [↗]
Olmsted syndrome [↗]
OMD [↗]
Omenn syndrome [↗]
OMM syndrome [↗]
Omodysplasia [↗]
Omphalocele [↗]
Omphalocele - cloacal exstrophy - imperforate anus - spinal defect [↗]
Omphalocele syndrome, Shprintzen-Goldberg type [↗]
Omphalomesenteric cyst [↗]
Onat syndrome [↗]
Onchocerciasis [↗]
Oncocytic cardiomyopathy [↗]
Ondine-Hirschsprung disease [↗]
Ondine-Hirschsprung syndrome [↗]
Ondine syndrome [↗]
ONMR syndrome [↗]
onycho-digito-mammary syndrome [↗]
Onychodystrophy - deafness [↗]
Onychodystrophy totalis [↗]
Onychoosteodysplasia [↗]
Onycho-tricho-dysplasia - neutropenia [↗]
Oochs syndrome [↗]
OOD [↗]
OPA2 [↗]
OPA3, autosomal dominant [↗]
Open iniencephaly [↗]
Ophthalmic ichthyosis [↗]
Ophthalmoacromelic syndrome [↗]
Ophthalmomandibulomelic dysplasia [↗]
Ophthalmoplegia - hypotonia - ataxia - hypoacusis - athetosis [↗]
Ophthalmoplegia - intellectual deficit - lingua scrotalis [↗]
Ophthalmoplegia - myalgia - tubular aggregates [↗]
Opitz BBB/G syndrome [↗]
Opitz-Caltabiano syndrome [↗]
Opitz-Frias syndrome [↗]
Opitz-Reynolds-FitzGerald syndrome [↗]
Opitz trigonocephaly-like syndrome [↗]
Opitz trigonocephaly syndrome [↗]
OPMD [↗]
Oppenheim's dystonia [↗]
OPPG [↗]
Opsismodysplasia [↗]
Opsoclonus-myoclonus syndrome [↗]
Optic atrophy [↗]
Optic atrophy - deafness- polyneuropathy - myopathy [↗]
Optic atrophy - ophthalmoplegia - ptosis - deafness - myopathy [↗]
Optic atrophy plus syndrome [↗]
Optic atrophy type 2 [↗]
Optic pathway glioma [↗]
Oral erosive lichen [↗]
Oral-facial-digital syndrome [↗]
Oral-facial-digital syndrome, Gabrielli type [↗]
Oral-facial-digital syndrome type 1 [↗]
Oral-facial-digital syndrome type 10 [↗]
Oral-facial-digital syndrome type 11 [↗]
Oral-facial-digital syndrome type 2 [↗]
Oral-facial-digital syndrome type 3 [↗]
Oral-facial-digital syndrome type 4 [↗]
Oral-facial-digital syndrome type 5 [↗]
Oral-facial-digital syndrome type 6 [↗]
Oral-facial-digital syndrome type 7 [↗]
Oral-facial-digital syndrome type 8 [↗]
Oral-facial-digital syndrome type 9 [↗]
Oral-facial-digital syndrome with retinal abnormalities [↗]
Oral-facial dyskinesia [↗]
Orbital cyst with cerebral and focal dermal malformations [↗]
Orbital leiomyoma [↗]
Orbital medulloepithelioma [↗]
Organic early-onset schizophrenia [↗]
Ormond's disease [↗]
Ornithine aminotransferase deficiency [↗]
Ornithine carbamoyltransferase deficiency [↗]
Ornithine transcarbamylase deficiency [↗]
Oroacral syndrome [↗]
Orocraniodigital syndrome [↗]
Orofaciodigital syndrome [↗]
Orofaciodigital syndrome, Gabrielli type [↗]
Orofaciodigital syndrome, Thurston type [↗]
Orofaciodigital syndrome type 1 [↗]
Orofaciodigital syndrome type 10 [↗]
Orofaciodigital syndrome type 11 [↗]
Orofaciodigital syndrome type 2 [↗]
Orofaciodigital syndrome type 3 [↗]
Orofaciodigital syndrome type 4 [↗]
Orofaciodigital syndrome type 5 [↗]
Orofaciodigital syndrome type 6 [↗]
Orofaciodigital syndrome type 7 [↗]
Orofaciodigital syndrome type 8 [↗]
Orofaciodigital syndrome type 9 [↗]
Orofaciodigital syndrome with fibular aplasia [↗]
Orofaciodigital syndrome with retinal abnormalities [↗]
Oromandibular dystonia [↗]
Oro-mandibular-limb hypogenesis syndrome [↗]
Oropharyngeal teratoma [↗]
Oroticaciduria [↗]
Orotidylic decarboxylase deficiency [↗]
Oroya fever [↗]
OSA syndrome [↗]
Osebold-Remondini syndrome [↗]
Osgood-Schlatter disease [↗]
OSLAM syndrome [↗]
Osler-Vaquez disease [↗]
OSMED [↗]
Osseous vascular malformation [↗]
Ossification anomalies - psychomotor development delay [↗]
Osteoblastoma [↗]
Osteochondritis dissecans and short stature [↗]
Osteochondritis of phalangeal epiphyses [↗]
Osteochondritis of tarsal/metatarsal bone [↗]
Osteochondritis of the capital femoral epiphysis [↗]
Osteochondritis of the lunate bone [↗]
Osteochondritis of the tibial tubercle [↗]
Osteochondrodysplatic dwarfism - deafness - retinitis pigmentosa [↗]
Osteochondrodysplatic nanism - deafness - retinitis pigmentosa [↗]
Osteo-chondro-muscular dystrophy [↗]
Osteochondrosis deformans tibiae [↗]
Osteochondrosis of patella [↗]
Osteochondrosis of phalangeal epiphyses [↗]
Osteochondrosis of the capital femoral epiphysis [↗]
Osteochondrosis of the capital humerus [↗]
Osteochondrosis of the lunate bone [↗]
Osteochondrosis of the tarsal bone [↗]
Osteochondrosis of the tibial tubercle [↗]
Osteocraniosplenic syndrome [↗]
Osteocraniostenosis [↗]
Osteodysplasty, Melnick-Needles type [↗]
Osteofibrous dysplasia [↗]
Osteogenesis imperfecta [↗]
Osteogenesis imperfecta - congenital joint contractures [↗]
Osteogenesis imperfecta - retinopathy - seizures - intellectual deficit [↗]
Osteogenesis imperfecta - shortened long bones - white sclerae [↗]
Osteogenesis imperfecta type 1 [↗]
Osteogenesis imperfecta type 2 [↗]
Osteogenesis imperfecta type 3 [↗]
Osteogenesis imperfecta type 4 [↗]
Osteogenesis imperfecta type 5 [↗]
Osteogenic sarcoma [↗]
Osteoglophonic dwarfism [↗]
Osteolysis hereditary multicentric [↗]
Osteomesopyknosis [↗]
Osteopathia striata - cranial sclerosis [↗]
Osteopathia striata - pigmentary dermopathy - white forelock [↗]
Osteopenia - intellectual deficit - sparse hair [↗]
Osteopenia - myopia - hearing loss - intellectual deficit - facial dysmorphism [↗]
Osteopetrosis autosomal dominant type 2 [↗]
Osteopetrosis - hypogammaglobulinemia [↗]
Osteopetrosis with renal tubular acidosis [↗]
Osteopoikilosis - short stature - intellectual deficit [↗]
Osteoporosis - macrocephaly - blindness - joint hyperlaxity [↗]
Osteoporosis-oculocutaneous-hypopigmentation syndrome [↗]
Osteoporosis - pseudoglioma [↗]
Osteopsathyrosis [↗]
Osteosarcoma [↗]
Osteosarcoma - limb anomalies - erythroid macrocytosis [↗]
Osteosclerosis - developmental delay - craniosynostosis [↗]
Osteosclerosis - ichthyosis - premature ovarian failure [↗]
Osteosclerotic myeloma [↗]
Ostravik-Lindemann-Solberg syndrome [↗]
O'Sullivan-McLeod syndrome [↗]
OTC deficency [↗]
Otodental dysplasia [↗]
Otodental syndrome [↗]
Otofaciocervical syndrome [↗]
Otomandibular dysostosis [↗]
Otomandibular syndrome [↗]
Oto-onycho-peroneal syndrome [↗]
Otopalatodigital syndrome [↗]
Otopalatodigital syndrome type 1 [↗]
Otopalatodigital syndrome type 2 [↗]
Otospondylomegaepiphyseal dysplasia [↗]
OTUDP syndrome [↗]
Ouvrier-Billson syndrome [↗]
Ovarian adenocarcinoma [↗]
Ovarian cancer of sex cord-stromal origin [↗]
Ovarian carcinosarcoma [↗]
Ovarian germ cell cancer [↗]
Ovarian germ cell malignant tumor [↗]
Ovarian gonadoblastoma [↗]
Ovarian hyperstimulation syndrome [↗]
Ovarian malignant Sertoli-Leydig cell tumor [↗]
Ovarian malignant tumor of sex cord-stromal origin [↗]
Ovarian Sertoli-Leydig cell cancer [↗]
Ovarian tumor of low malignant potential [↗]
Ovarioleukodystrophy [↗]
Overgrowth - craniosynostosis - arthrogryposis [↗]
Overhydrated hereditary stomatocytosis [↗]
Overlap myositis [↗]
Ovotesticular disorder of sex development [↗]
Ovotesticular DSD [↗]
Owren's disease [↗]
Oxoglutaricaciduria [↗]
Oxysterol 7-alpha-hydroxylase deficiency [↗]

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