List of genes available initial O

List of genes available for sequencing

myGenomics specializes in custom target sequencing and can develop any gene or panel of genes of interest. Some of the genes available are listed below.

List adopted from Genetics Home Reference: A Guide to Understanding genetic Conditions

• OA, see ocular albinism
• OAS, see ophthalmo-acromelic syndrome
• OAT deficiency, see gyrate atrophy of the choroid and retina
• OAV complex, see craniofacial microsomia
• OAVS, see craniofacial microsomia
• Oberklaid-Danks syndrome, see Bohring-Opitz syndrome
• obesity due to congenital leptin deficiency, see congenital leptin deficiency
• obesity due to leptin receptor gene deficiency, see leptin receptor deficiency
• obesity, early-onset, adrenal insufficiency, and red hair, see proopiomelanocortin deficiency
• obesity, morbid, due to leptin deficiency, see congenital leptin deficiency
• obesity, morbid, due to leptin receptor deficiency, see leptin receptor deficiency
• obesity, morbid, nonsyndromic 1, see congenital leptin deficiency
• obesity, morbid, nonsyndromic 2, see leptin receptor deficiency
• obesity, severe, due to leptin deficiency, see congenital leptin deficiency
• obesity-hypotonia syndrome, see Cohen syndrome
• obstetric cholestasis, see intrahepatic cholestasis of pregnancy
• obstructive disease of the pulmonary veins, see pulmonary veno-occlusive disease
• OCA, see oculocutaneous albinism
• occlusive infantile arteriopathy, see generalized arterial calcification of infancy
• occupational cramp, see task-specific focal dystonia
• occupational dystonia, see task-specific focal dystonia
• OCD, see familial osteochondritis dissecans
• Ochoa syndrome
• ocular albinism
• ocular coloboma, see coloboma
• ocular retraction syndrome, see isolated Duane retraction syndrome
• oculo-dento-digital dysplasia, see oculodentodigital dysplasia
• oculo-dento-osseous dysplasia, see oculodentodigital dysplasia
• oculo-digito-esophagoduodental (ODED) syndrome, see Feingold syndrome
• Oculo-facio-cardio-dental syndrome, see oculofaciocardiodental syndrome
• oculo-oto-facial dysplasia, see Burn-McKeown syndrome
• oculo-skeletal-abdominal syndrome, see 3MC syndrome
• oculoauriculovertebral spectrum, see craniofacial microsomia
• oculocerebrofacial syndrome, Kaufman type, see Kaufman oculocerebrofacial syndrome
• oculocerebrorenal syndrome, see Lowe syndrome
• oculocerebrorenal syndrome of Lowe, see Lowe syndrome
• oculocutaneous albinism
• oculocutaneous albinism with leukocyte defect, see Chediak-Higashi syndrome
• oculodentodigital dysplasia
• oculodentodigital syndrome, see oculodentodigital dysplasia
• oculodentoosseous dysplasia, see oculodentodigital dysplasia
• oculofaciocardiodental syndrome
• Oculogastrointestinal muscular dystrophy, see mitochondrial neurogastrointestinal encephalopathy disease
• oculootofacial dysplasia, see Burn-McKeown syndrome
• oculopalatoskeletal syndrome, see 3MC syndrome
• Oculopharyngeal dystrophy, see oculopharyngeal muscular dystrophy
• oculopharyngeal muscular dystrophy
• oculosympathetic palsy, see Horner syndrome
• OD, see familial osteochondritis dissecans
• ODD syndrome, see oculodentodigital dysplasia
• ODDD, see oculodentodigital dysplasia
• ODOD, see oculodentodigital dysplasia
• odontoleukodystrophy, see Pol III-related leukodystrophy
• oestrogen synthetase deficiency, see aromatase deficiency
• OFCD syndrome, see oculofaciocardiodental syndrome
• OFDS, see oral-facial-digital syndrome
• OGD, see osteoglophonic dysplasia
• OGIMD, see mitochondrial neurogastrointestinal encephalopathy disease
• Ohaha syndrome, see infantile-onset spinocerebellar ataxia
• Ohdo syndrome, Maat-Kievit-Brunner type
• Ohdo syndrome, MKB type, see Ohdo syndrome, Maat-Kievit-Brunner type
• Ohdo syndrome, Say-Barber-Biesecker variant, see Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant
• Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant
• Ohdo syndrome, SBBYS variant, see Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant
• OI, see osteogenesis imperfecta
• Okihiro syndrome, see Duane-radial ray syndrome
• OKS, see FG syndrome
• OKT deficiency, see gyrate atrophy of the choroid and retina
• Old Silk Route disease, see Behçet disease
• old-aged sensorineural hearing impairment, see age-related hearing loss
• Oligophrenia microphthalmus, see Norrie disease
• olivopontocerebellar atrophy I, see spinocerebellar ataxia type 1
• Ollier disease
• Ollier’s syndrome, see Ollier disease
• Omenn syndrome
• Omenn’s syndrome, see Omenn syndrome
• omphalocele, see abdominal wall defect
• ONCR, see renal coloboma syndrome
• Ondine Syndrome, see congenital central hypoventilation syndrome
• Ondine-Hirschsprung disease, see congenital central hypoventilation syndrome
• onychauxis, hyponychia, and onycholysis, see nonsyndromic congenital nail disorder 10
• OOFD, see Burn-McKeown syndrome
• OPA3 defect, see Costeff syndrome
• OPCA, see multiple system atrophy
• OPCH, see pontocerebellar hypoplasia
• OPD syndrome, type 1, see otopalatodigital syndrome type 1
• OPD syndrome, type 2, see otopalatodigital syndrome type 2
• open spine, see spina bifida
• ophthalmo-acromelic syndrome
• ophthalmoacromelic syndrome, see ophthalmo-acromelic syndrome
• ophthalmoplegia, hypotonia, ataxia, hypacusis, and athetosis, see infantile-onset spinocerebellar ataxia
• ophthalmoplegia, progressive external, and scoliosis, see horizontal gaze palsy with progressive scoliosis
• Opitz BBB syndrome, see Opitz G/BBB syndrome
• Opitz BBB/G syndrome, see Opitz G/BBB syndrome
• Opitz G syndrome, see Opitz G/BBB syndrome
• Opitz G/BBB syndrome
• Opitz syndrome, see Opitz G/BBB syndrome
• Opitz trigonocephaly-like syndrome, see Bohring-Opitz syndrome
• Opitz-Frias syndrome, see Opitz G/BBB syndrome
• Opitz-Kaveggia syndrome, see FG syndrome
• OPMD, see oculopharyngeal muscular dystrophy
• Oppenheim dystonia, see early-onset primary dystonia
• Oppenheim’s dystonia, see early-onset primary dystonia
• OPPG, see osteoporosis-pseudoglioma syndrome
• optic atrophy plus syndrome, see Costeff syndrome
• optic atrophy type 1
• optic atrophy, autosomal dominant, see optic atrophy type 1
• optic atrophy, hereditary, autosomal dominant, see optic atrophy type 1
• optic atrophy, juvenile, see optic atrophy type 1
• optic atrophy, Kjer type, see optic atrophy type 1
• optic coloboma, vesicoureteral reflux, and renal anomalies, see renal coloboma syndrome
• optic nerve coloboma renal syndrome, see renal coloboma syndrome
• optic-spinal MS, see neuromyelitis optica
• opticospinal MS, see neuromyelitis optica
• oral-facial-digital syndrome
• oral-mandibular-auricular syndrome, see craniofacial microsomia
• ORAS, see otulipenia
• Ormond disease, see retroperitoneal fibrosis
• Ormond’s disease, see retroperitoneal fibrosis
• ornithine aminotransferase deficiency, see gyrate atrophy of the choroid and retina
• Ornithine Carbamoyltransferase Deficiency Disease, see ornithine transcarbamylase deficiency
• ornithine keto acid aminotransferase deficiency, see gyrate atrophy of the choroid and retina
• ornithine transcarbamylase deficiency
• ornithine translocase deficiency
• ornithine-delta-aminotransferase deficiency, see gyrate atrophy of the choroid and retina
• Ornithinemia with gyrate atrophy, see gyrate atrophy of the choroid and retina
• oro-facio-digital syndrome, see oral-facial-digital syndrome
• orodigitofacial dysostosis, see oral-facial-digital syndrome
• orodigitofacial syndrome, see oral-facial-digital syndrome
• orofaciodigital syndrome, see oral-facial-digital syndrome
• OSA syndrome, see 3MC syndrome
• Osler-Vaquez disease, see polycythemia vera
• Osler-Weber-Rendu syndrome, see hereditary hemorrhagic telangiectasia
• OSMED, see otospondylomegaepiphyseal dysplasia
• osseous Paget’s disease, see Paget disease of bone
• osseous-oculo-dental dysplasia, see oculodentodigital dysplasia
• osteitis deformans, see Paget disease of bone
• osteitis fibrosa disseminata, see McCune-Albright syndrome
• osteochalasia desmalis familiaris, see juvenile Paget disease
• osteochondritis dissecans, short stature, and early-onset osteoarthritis, see familial osteochondritis dissecans
• osteodermia, see progressive osseous heteroplasia
• osteodysplastic primordial dwarfism type II, see microcephalic osteodysplastic primordial dwarfism type II
• osteodysplasty of Melnick and Needles, see Melnick-Needles syndrome
• osteoectasia with hyperphosphatasia, see juvenile Paget disease
• osteogenesis imperfecta
• osteogenesis imperfecta with unusual skeletal lesions, see gnathodiaphyseal dysplasia
• osteogenesis imperfecta, Levin type, see gnathodiaphyseal dysplasia
• osteogenesis imperfecta, ocular form, see osteoporosis-pseudoglioma syndrome
• osteoglophonic dwarfism, see osteoglophonic dysplasia
• osteoglophonic dysplasia
• osteoma cutis, see progressive osseous heteroplasia
• osteopathia condensans disseminata, see Buschke-Ollendorff syndrome
• osteopetroses, see osteopetrosis
• osteopetrosis
• osteoporosis-pseudoglioma syndrome
• osteosis cutis, see progressive osseous heteroplasia
• Osterreicher syndrome, see nail-patella syndrome
• oto-palato-digital syndrome, type I, see otopalatodigital syndrome type 1
• oto-palato-digital syndrome, type II, see otopalatodigital syndrome type 2
• oto-spondylo-megaepiphyseal dysplasia, see otospondylomegaepiphyseal dysplasia
• otogenic vertigo, see Ménière disease
• otomandibular dysostosis, see craniofacial microsomia
• otopalatodigital syndrome type 1
• otopalatodigital syndrome type 2
• otospondylomegaepiphyseal dysplasia
• OTULIN-related autoinflammatory syndrome, see otulipenia
• otulipenia
• ovarian cancer
• ovarian carcinoma, see ovarian cancer
• ovarian dysgenesis with sensorineural deafness, see Perrault syndrome
• Owren disease, see factor V deficiency
• Owren’s disease, see factor V deficiency
• oxalosis, see primary hyperoxaluria
• oxaluria, primary, see primary hyperoxaluria