Human Disease Vocabulary Browser

The current vocabulary contains human disease, syndrome, and condition terms from Online Mendelian Inheritance in Man (OMIM database).

Browse vocabulary terms by beginning character

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Human Diseases/Syndromes Beginning with "O"

To see all annotations for a disease, click the disease name.

OMIM ID	Human Disease
OMIM:601665	Obesity
OMIM:620195	Obesity and Hypopigmentation; OBHP
OMIM:609734	Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair; OBAIRH
OMIM:613886	Obesity, Hyperphagia, and Developmental Delay; OBHD
OMIM:257500	Obesity-Hypoventilation Syndrome
OMIM:164230	Obsessive-Compulsive Disorder; OCD
OMIM:310900	Occipital Hair, White Lock of
OMIM:304150	Occipital Horn Syndrome; OHS
OMIM:613587	Occult Macular Dystrophy; OCMD
OMIM:164185	Ocular Cicatricial Pemphigoid; OCP
OMIM:164190	Ocular Dominance
OMIM:257550	Ocular Motor Apraxia
OMIM:257600	Ocular Myopathy with Curare Sensitivity
OMIM:600510	Ocular Pigment Dispersion with or without Glaucoma; OPDG
OMIM:612109	Oculoauricular Syndrome; OCACS
OMIM:601452	Oculoauriculofrontonasal Syndrome; OAFNS
OMIM:257790	Oculocerebral Hypopigmentation Syndrome of Preus
OMIM:257800	Oculocerebral Syndrome with Hypopigmentation
OMIM:164180	Oculocerebrocutaneous Syndrome
OMIM:619165	Oculocutaneous Albinism, Type Viii; OCA8
OMIM:257850	Oculodentodigital Dysplasia, Autosomal Recessive
OMIM:164200	Oculodentodigital Dysplasia; ODDD
OMIM:600268	Oculoectodermal Syndrome; OES
OMIM:619318	Oculogastrointestinal Neurodevelopmental Syndrome; OGIN
OMIM:604301	Oculomedin; OCLM
OMIM:619215	Oculomotor-Abducens Synkinesis; OCABSN
OMIM:151610	Oculomotor-Levator Synkinesis; OCLEVS
OMIM:257910	Oculopalatocerebral Syndrome
OMIM:164300	Oculopharyngeal Muscular Dystrophy 1; OPMD1
OMIM:620460	Oculopharyngeal Muscular Dystrophy 2; OPMD2
OMIM:618637	Oculopharyngeal Myopathy with Leukoencephalopathy 1; OPML1
OMIM:164310	Oculopharyngodistal Myopathy 1; OPDM1
OMIM:618940	Oculopharyngodistal Myopathy 2; OPDM2
OMIM:619473	Oculopharyngodistal Myopathy 3; OPDM3
OMIM:619790	Oculopharyngodistal Myopathy 4; OPDM4
OMIM:257970	Oculorenocerebellar Syndrome
OMIM:618440	Oculoskeletodental Syndrome; OCSKD
OMIM:257960	Oculotrichodysplasia; OTD
OMIM:618512	O'donnell-Luria-Rodan Syndrome; ODLURO
OMIM:184260	Odontochondrodysplasia 1; ODCD1
OMIM:619269	Odontochondrodysplasia 2 with Hearing Loss and Diabetes; ODCD2
OMIM:613628	Odontoid Hypoplasia
OMIM:164330	Odontoma-Dysphagia Syndrome
OMIM:601319	Odontomicronychial Dysplasia
OMIM:257980	Odontoonychodermal Dysplasia; OODD
OMIM:601957	Odontotrichoungual-Digital-Palmar Syndrome
OMIM:258040	Oeis Complex
OMIM:300855	Ogden Syndrome; OGDNS
OMIM:258100	Oguchi Disease 1
OMIM:613411	Oguchi Disease 2
OMIM:249620	Ohdo Syndrome
OMIM:603736	Ohdo Syndrome, Sbbys Variant; SBBYSS
OMIM:300895	Ohdo Syndrome, X-Linked; OHDOX
OMIM:613949	Okt4 Epitope Deficiency; OKT4D
OMIM:617062	Okur-Chung Neurodevelopmental Syndrome; OCNDS
OMIM:608615	Oligodontia-Colorectal Cancer Syndrome; ODCRCS
OMIM:275400	Oliver-Mcfarlane Syndrome; OMCS
OMIM:258200	Oliver Syndrome
OMIM:614594	Olmsted Syndrome 1; OLMS1
OMIM:619208	Olmsted Syndrome 2; OLMS2
OMIM:300918	Olmsted Syndrome, X-Linked; OLMSX
OMIM:603554	Omenn Syndrome
OMIM:258315	Omodysplasia 1; OMOD1
OMIM:164745	Omodysplasia 2; OMOD2
OMIM:164750	Omphalocele, Autosomal
OMIM:258320	Omphalocele-Cleft Palate Syndrome, Lethal
OMIM:609545	Omphalocele, Diaphragmatic Hernia, and Radial Ray Defects
OMIM:310980	Omphalocele, X-Linked
OMIM:553000	Oncocytoma
OMIM:619356	Onychodystrophy, Osteodystrophy, Impaired Intellectual Development, and Seizures Syndrome; OORS
OMIM:164680	Onychogryposis, Pedal, with Keratosis Plantaris and Coarse Hair
OMIM:258360	Onychotrichodysplasia and Neutropenia
OMIM:619176	Oocyte/Zygote/Embryo Maturation Arrest 10; OZEMA10
OMIM:619643	Oocyte/Zygote/Embryo Maturation Arrest 11; OZEMA11
OMIM:619697	Oocyte/Zygote/Embryo Maturation Arrest 12; OZEMA12
OMIM:620154	Oocyte/Zygote/Embryo Maturation Arrest 13; OZEMA13
OMIM:620276	Oocyte/Zygote/Embryo Maturation Arrest 14; OZEMA14
OMIM:616814	Oocyte/Zygote/Embryo Maturation Arrest 15; OZEMA15
OMIM:617234	Oocyte/Zygote/Embryo Maturation Arrest 16; OZEMA16
OMIM:620319	Oocyte/Zygote/Embryo Maturation Arrest 17; OZEMA17
OMIM:620332	Oocyte/Zygote/Embryo Maturation Arrest 18; OZEMA18
OMIM:620333	Oocyte/Zygote/Embryo Maturation Arrest 19; OZEMA19
OMIM:615774	Oocyte/Zygote/Embryo Maturation Arrest 1; OZEMA1
OMIM:620383	Oocyte/Zygote/Embryo Maturation Arrest 20; OZEMA20
OMIM:620610	Oocyte/Zygote/Embryo Maturation Arrest 21; OZEMA21
OMIM:616780	Oocyte/Zygote/Embryo Maturation Arrest 2; OZEMA2
OMIM:617712	Oocyte/Zygote/Embryo Maturation Arrest 3; OZEMA3
OMIM:617743	Oocyte/Zygote/Embryo Maturation Arrest 4; OZEMA4
OMIM:617996	Oocyte/Zygote/Embryo Maturation Arrest 5; OZEMA5
OMIM:618353	Oocyte/Zygote/Embryo Maturation Arrest 6; OZEMA6
OMIM:618550	Oocyte/Zygote/Embryo Maturation Arrest 7; OZEMA7
OMIM:619009	Oocyte/Zygote/Embryo Maturation Arrest 8; OZEMA8
OMIM:619011	Oocyte/Zygote/Embryo Maturation Arrest 9; OZEMA9
OMIM:164900	Ophthalmomandibulomelic Dysplasia
OMIM:311000	Ophthalmoplegia, External, and Myopia; OPEM
OMIM:618155	Ophthalmoplegia, External, with Rib and Vertebral Anomalies; EORVA
OMIM:165000	Ophthalmoplegia, Familial Static
OMIM:165098	Ophthalmoplegia, Familial Total, with Iris Transillumination
OMIM:165150	Ophthalmoplegia, Progressive, with Scrotal Tongue and Mental Deficiency
OMIM:258400	Ophthalmoplegia Totalis with Ptosis and Miosis
OMIM:258470	Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria
OMIM:610064	Opioid Dependence, Susceptibility to, 1
OMIM:300000	Opitz Gbbb Syndrome; GBBB
OMIM:305450	Opitz-Kaveggia Syndrome; OKS
OMIM:258480	Opsismodysplasia; OPSMD
OMIM:616732	Optic Atrophy 10 with or without Ataxia, Impaired Intellectual Development, and Seizures; OPA10
OMIM:617302	Optic Atrophy 11; OPA11
OMIM:618977	Optic Atrophy 12; OPA12
OMIM:165510	Optic Atrophy 13 with Retinal and Foveal Abnormalities; OPA13
OMIM:620550	Optic Atrophy 14; OPA14
OMIM:620583	Optic Atrophy 15; OPA15
OMIM:620629	Optic Atrophy 16; OPA16
OMIM:165500	Optic Atrophy 1; OPA1
OMIM:311050	Optic Atrophy 2; OPA2
OMIM:165300	Optic Atrophy 3, Autosomal Dominant; OPA3
OMIM:605293	Optic Atrophy 4; OPA4
OMIM:610708	Optic Atrophy 5; OPA5
OMIM:258500	Optic Atrophy 6; OPA6
OMIM:612989	Optic Atrophy 7 with or without Auditory Neuropathy; OPA7
OMIM:616648	Optic Atrophy 8; OPA8
OMIM:616289	Optic Atrophy 9; OPA9
OMIM:165199	Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant
OMIM:258650	Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Recessive
OMIM:311100	Optic Atrophy--Spastic Paraplegia Syndrome
OMIM:165200	Optic Atrophy with Demyelinating Disease of Cns
OMIM:125250	Optic Atrophy with or without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy
OMIM:212550	Optic Disc Anomalies with Retinal and/or Macular Dystrophy; ODRMD
OMIM:165550	Optic Nerve Hypoplasia, Bilateral
OMIM:258700	Opticocochleodentate Degeneration
OMIM:258840	Oral and Digital Anomalies with Ichthyosis
OMIM:258800	Oral Sensibility, Disturbance of
OMIM:165600	Orbital Margin, Hypoplasia of
OMIM:311250	Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to
OMIM:603446	Oroacral Syndrome, Verloes-Koulischer Type
OMIM:613705	Orofacial Cleft 10; OFC10
OMIM:600625	Orofacial Cleft 11; OFC11
OMIM:612858	Orofacial Cleft 12; OFC12
OMIM:613857	Orofacial Cleft 13; OFC13
OMIM:615892	Orofacial Cleft 14; OFC14
OMIM:616788	Orofacial Cleft 15; OFC15
OMIM:119530	Orofacial Cleft 1; OFC1
OMIM:602966	Orofacial Cleft 2; OFC2
OMIM:600757	Orofacial Cleft 3; OFC3
OMIM:608371	Orofacial Cleft 4; OFC4
OMIM:608874	Orofacial Cleft 5; OFC5
OMIM:608864	Orofacial Cleft 6, Susceptibility To; OFC6
OMIM:618149	Orofacial Cleft 8; OFC8
OMIM:610361	Orofacial Cleft 9; OFC9
OMIM:258850	Orofaciodigital Syndrome III; OFD3
OMIM:252100	Orofaciodigital Syndrome II; OFD2
OMIM:311200	Orofaciodigital Syndrome I; OFD1
OMIM:258860	Orofaciodigital Syndrome IV; OFD4
OMIM:258865	Orofaciodigital Syndrome IX; OFD9
OMIM:300484	Orofaciodigital Syndrome Viii; OFD8
OMIM:608518	Orofaciodigital Syndrome VII; OFD7
OMIM:277170	Orofaciodigital Syndrome VI; OFD6
OMIM:174300	Orofaciodigital Syndrome V; OFD5
OMIM:612913	Orofaciodigital Syndrome XI; OFD11
OMIM:615948	Orofaciodigital Syndrome Xiv; OFD14
OMIM:620107	Orofaciodigital Syndrome XIX; OFD19
OMIM:165590	Orofaciodigital Syndrome X; OFD10
OMIM:617927	Orofaciodigital Syndrome Xviii; OFD18
OMIM:617926	Orofaciodigital Syndrome Xvii; OFD17
OMIM:617563	Orofaciodigital Syndrome Xvi; OFD16
OMIM:617127	Orofaciodigital Syndrome Xv; OFD15
OMIM:620718	Orofaciodigital Syndrome Xx; OFD20
OMIM:258900	Orotic Aciduria
OMIM:223360	Orthostatic Hypotension 1; ORTHYP1
OMIM:618182	Orthostatic Hypotension 2; ORTHYP2
OMIM:143850	Orthostatic Hypotensive Disorder, Streeten Type
OMIM:604715	Orthostatic Intolerance
OMIM:112910	Osebold-Remondini Syndrome
OMIM:603389	Osebold Skeletal Dysplasia/Osteolysis Syndrome
OMIM:165660	Oslam Syndrome
OMIM:166350	Osseous Heteroplasia, Progressive; POH
OMIM:165680	Ossicular Malformations, Familial
OMIM:602475	Ossification of the Posterior Longitudinal Ligament of Spine; OPLL
OMIM:165670	Ossified Ear Cartilages
OMIM:165720	Osteoarthritis Susceptibility 1; OS1
OMIM:140600	Osteoarthritis Susceptibility 2; OS2
OMIM:607850	Osteoarthritis Susceptibility 3; OS3
OMIM:610839	Osteoarthritis Susceptibility 4; OS4
OMIM:612400	Osteoarthritis Susceptibility 5; OS5
OMIM:612401	Osteoarthritis Susceptibility 6; OS6
OMIM:604864	Osteoarthritis with Mild Chondrodysplasia; OSCDP
OMIM:618167	Osteochondrodysplasia, Brachydactyly, and Overlapping Malformed Digits; OCBMD
OMIM:616897	Osteochondrodysplasia, Complex Lethal, Symoens-Barnes-Gistelinck Type;
OMIM:166990	Osteochondrodysplasia, Rhizomelic, with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension
OMIM:259250	Osteodysplasia, Familial, Anderson Type
OMIM:259270	Osteodysplasty, Precocious, of Danks, Mayne, and Kozlowski
OMIM:607278	Osteofibrous Dysplasia, Susceptibility To; OSFD
OMIM:259410	Osteogenesis Imperfecta Congenita, Microcephaly, and Cataracts
OMIM:259420	Osteogenesis Imperfecta, Type III; OI3
OMIM:166210	Osteogenesis Imperfecta, Type II; OI2
OMIM:166200	Osteogenesis Imperfecta, Type I; OI1
OMIM:166220	Osteogenesis Imperfecta, Type IV; OI4
OMIM:259440	Osteogenesis Imperfecta, Type IX; OI9
OMIM:610915	Osteogenesis Imperfecta, Type Viii; OI8
OMIM:610682	Osteogenesis Imperfecta, Type VII; OI7
OMIM:613982	Osteogenesis Imperfecta, Type VI; OI6
OMIM:610967	Osteogenesis Imperfecta, Type V; OI5
OMIM:614856	Osteogenesis Imperfecta, Type Xiii; OI13
OMIM:613849	Osteogenesis Imperfecta, Type Xii; OI12
OMIM:610968	Osteogenesis Imperfecta, Type XI; OI11
OMIM:615066	Osteogenesis Imperfecta, Type Xiv; OI14
OMIM:301014	Osteogenesis Imperfecta, Type XIX; OI19
OMIM:613848	Osteogenesis Imperfecta, Type X; OI10
OMIM:617952	Osteogenesis Imperfecta, Type Xviii; OI18
OMIM:616507	Osteogenesis Imperfecta, Type Xvii; OI17
OMIM:616229	Osteogenesis Imperfecta, Type Xvi; OI16
OMIM:615220	Osteogenesis Imperfecta, Type Xv; OI15
OMIM:620639	Osteogenesis Imperfecta, Type Xxiii; OI23
OMIM:619795	Osteogenesis Imperfecta, Type Xxii; OI22
OMIM:619131	Osteogenesis Imperfecta, Type Xxi; OI21
OMIM:618644	Osteogenesis Imperfecta, Type Xx; OI20
OMIM:166230	Osteogenesis Imperfecta with Opalescent Teeth, Blue Sclerae and Wormian Bones, but without Fractures
OMIM:259500	Osteogenic Sarcoma
OMIM:166250	Osteoglophonic Dysplasia; OGD
OMIM:259550	Osteoid Osteoma
OMIM:259610	Osteolysis Syndrome, Recessive
OMIM:603600	Osteoma of Cranial Vault, Familial
OMIM:259650	Osteoma of Middle Ear
OMIM:166400	Osteomas of Mandible
OMIM:166450	Osteomesopyknosis
OMIM:619377	Osteootohepatoenteric Syndrome; OOHE
OMIM:300373	Osteopathia Striata with Cranial Sclerosis; OSCS
OMIM:259690	Osteopenia and Sparse Hair
OMIM:600329	Osteopetrosis and Infantile Neuroaxonal Dystrophy
OMIM:607634	Osteopetrosis, Autosomal Dominant 1; OPTA1
OMIM:166600	Osteopetrosis, Autosomal Dominant 2; OPTA2
OMIM:618107	Osteopetrosis, Autosomal Dominant 3; OPTA3
OMIM:259700	Osteopetrosis, Autosomal Recessive 1; OPTB1
OMIM:259710	Osteopetrosis, Autosomal Recessive 2; OPTB2
OMIM:259730	Osteopetrosis, Autosomal Recessive 3; OPTB3
OMIM:611490	Osteopetrosis, Autosomal Recessive 4; OPTB4
OMIM:259720	Osteopetrosis, Autosomal Recessive 5; OPTB5
OMIM:611497	Osteopetrosis, Autosomal Recessive 6; OPTB6
OMIM:612301	Osteopetrosis, Autosomal Recessive 7; OPTB7
OMIM:615085	Osteopetrosis, Autosomal Recessive 8; OPTB8
OMIM:620366	Osteopetrosis, Autosomal Recessive 9; OPTB9
OMIM:166705	Osteopoikilosis and Dacryocystitis
OMIM:166710	Osteoporosis
OMIM:601220	Osteoporosis and Oculocutaneous Hypopigmentation Syndrome; OOCH
OMIM:619884	Osteoporosis, Childhood- or Juvenile-Onset, with Developmental Delay;
OMIM:259750	Osteoporosis, Juvenile
OMIM:259770	Osteoporosis-Pseudoglioma Syndrome; OPPG
OMIM:166740	Osteosclerosis with Ichthyosis and Fractures
OMIM:609993	Osteosclerosis with Ichthyosis and Premature Ovarian Failure
OMIM:603393	Osteosclerotic Chondrodysplasia, Lethal, with Intracellular Inclusions
OMIM:615198	Osteosclerotic Metaphyseal Dysplasia; OSMD
OMIM:166760	Otitis Media, Susceptibility To; OMS
OMIM:166750	Otodental Dysplasia
OMIM:166780	Otofaciocervical Syndrome 1; OTFCS
OMIM:615560	Otofaciocervical Syndrome 2, with T-Cell Deficiency; OTFCS2
OMIM:601976	Otofacioosseous-Gonadal Syndrome
OMIM:259780	Otoonychoperoneal Syndrome
OMIM:304120	Otopalatodigital Syndrome, Type II; OPD2
OMIM:311300	Otopalatodigital Syndrome, Type I; OPD1
OMIM:615589	Otosclerosis 10; OTSC10
OMIM:620576	Otosclerosis 11; OTSC11
OMIM:166800	Otosclerosis 1; OTSC1
OMIM:605727	Otosclerosis 2; OTSC2
OMIM:608244	Otosclerosis 3; OTSC3
OMIM:611571	Otosclerosis 4; OTSC4
OMIM:608787	Otosclerosis 5; OTSC5
OMIM:611572	Otosclerosis 7; OTSC7
OMIM:612096	Otosclerosis 8; OTSC8
OMIM:184840	Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant; OSMEDA
OMIM:215150	Otospondylomegaepiphyseal Dysplasia, Autosomal Recessive; OSMEDB
OMIM:311350	Ouabain Resistance; OUBR
OMIM:166910	Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis
OMIM:166900	Ovalocytosis, Southeast Asian; SAO
OMIM:167000	Ovarian Cancer
OMIM:607893	Ovarian Cancer, Susceptibility to, 1; OVCAS1
OMIM:619834	Ovarian Dysgenesis 10; ODG10
OMIM:233300	Ovarian Dysgenesis 1; ODG1
OMIM:300510	Ovarian Dysgenesis 2; ODG2
OMIM:614324	Ovarian Dysgenesis 3; ODG3
OMIM:616185	Ovarian Dysgenesis 4; ODG4
OMIM:617690	Ovarian Dysgenesis 5; ODG5
OMIM:618078	Ovarian Dysgenesis 6; ODG6
OMIM:618117	Ovarian Dysgenesis 7; ODG7
OMIM:618187	Ovarian Dysgenesis 8; ODG8
OMIM:619665	Ovarian Dysgenesis 9; ODG9
OMIM:605756	Ovarian Dysgenesis, Hypergonadotropic, with Short Stature and Recurrent Metabolic Acidosis
OMIM:166970	Ovarian Fibromata
OMIM:603737	Ovarian Germ Cell Cancer
OMIM:608115	Ovarian Hyperstimulation Syndrome; OHSS
OMIM:185000	Overhydrated Hereditary Stomatocytosis; OHST
OMIM:203740	Oxoglutarate Dehydrogenase Deficiency; OGDHD

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