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
601665	Obesity (59 mouse models)
613886	Obesity, Hyperphagia, and Developmental Delay
257500	Obesity-Hypoventilation Syndrome
164230	Obsessive-Compulsive Disorder; OCD (5 mouse models)
310900	Occipital Hair, White Lock of
304150	Occipital Horn Syndrome; OHS
613587	Occult Macular Dystrophy; OCMD
164185	Ocular Cicatricial Pemphigoid; OCP
164190	Ocular Dominance
257550	Ocular Motor Apraxia
257600	Ocular Myopathy with Curare Sensitivity
612109	Oculoauricular Syndrome (2 mouse models)
601452	Oculoauriculofrontonasal Syndrome; OAFNS
257790	Oculocerebral Hypopigmentation Syndrome of Preus
257800	Oculocerebral Syndrome with Hypopigmentation
164180	Oculocerebrocutaneous Syndrome
257850	Oculodentodigital Dysplasia, Autosomal Recessive
164200	Oculodentodigital Dysplasia; ODDD (5 mouse models)
610332	Oculootofacial Dysplasia
257910	Oculopalatocerebral Syndrome (1 mouse model)
164300	Oculopharyngeal Muscular Dystrophy; OPMD (2 mouse models)
164310	Oculopharyngodistal Myopathy; OPDM
257970	Oculorenocerebellar Syndrome
257960	Oculotrichodysplasia; OTD
613628	Odontoid Hypoplasia
164330	Odontoma-Dysphagia Syndrome
601319	Odontomicronychial Dysplasia
257980	Odontoonychodermal Dysplasia; OODD
601957	Odontotrichoungual-Digital-Palmar Syndrome
606632	Odor, Male, Women's Choice of
258040	Oeis Complex
300855	Ogden Syndrome; OGDNS
258100	Oguchi Disease 1
613411	Oguchi Disease 2 (1 mouse model)
249620	Ohdo Syndrome
603736	Ohdo Syndrome, Sbbys Variant; SBBYSS
613949	Okt4 Epitope Deficiency
608615	Oligodontia-Colorectal Cancer Syndrome; ODCRCS
258200	Oliver Syndrome
258300	Olivopontocerebellar Atrophy II, Autosomal Recessive
164700	Olivopontocerebellar Atrophy V; OPCA V
603554	Omenn Syndrome (1 mouse model)
258315	Omodysplasia 1; OMOD1
164745	Omodysplasia 2; OMOD2
164750	Omphalocele, Autosomal (1 mouse model)
258320	Omphalocele-Cleft Palate Syndrome, Lethal
609545	Omphalocele, Diaphragmatic Hernia, and Radial Ray Defects
310980	Omphalocele, X-Linked
553000	Oncocytoma
164891	Oncogene Yuasa
164680	Onychogryposis, Pedal, with Keratosis Plantaris and Coarse Hair
258360	Onychotrichodysplasia and Neutropenia
164900	Ophthalmomandibulomelic Dysplasia
311000	Ophthalmoplegia, External, and Myopia; OPEM
165000	Ophthalmoplegia, Familial Static
165098	Ophthalmoplegia, Familial Total, with Iris Transillumination
165150	Ophthalmoplegia, Progressive, with Scrotal Tongue and Mental Deficiency
258400	Ophthalmoplegia Totalis with Ptosis and Miosis
258470	Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria
610064	Opioid Dependence, Susceptibility to, 1
145410	Opitz Gbbb Syndrome, Autosomal Dominant
300000	Opitz Gbbb Syndrome, X-Linked (1 mouse model)
305450	Opitz-Kaveggia Syndrome; OKS
258480	Opsismodysplasia; OPSMD
165500	Optic Atrophy 1; OPA1 (3 mouse models)
311050	Optic Atrophy 2; OPA2
165300	Optic Atrophy 3, Autosomal Dominant
605293	Optic Atrophy 4; OPA4
610708	Optic Atrophy 5; OPA5
258500	Optic Atrophy 6; OPA6
612989	Optic Atrophy 7; OPA7
165199	Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant
258650	Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Recessive
311100	Optic Atrophy--Spastic Paraplegia Syndrome
165200	Optic Atrophy with Demyelinating Disease of Cns
165510	Optic Atrophy with Negative Electroretinograms
125250	Optic Atrophy with or without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy
165550	Optic Nerve Hypoplasia, Bilateral
311150	Opticoacoustic Nerve Atrophy with Dementia
258700	Opticocochleodentate Degeneration
258840	Oral and Digital Anomalies with Ichthyosis
258800	Oral Sensibility, Disturbance of
165600	Orbital Margin, Hypoplasia of
311250	Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to (7 mouse models)
603446	Oroacral Syndrome, Verloes-Koulischer Type
613705	Orofacial Cleft 10; OFC10
600625	Orofacial Cleft 11; OFC11
612858	Orofacial Cleft 12; OFC12
613857	Orofacial Cleft 13; OFC13
119530	Orofacial Cleft 1; OFC1
602966	Orofacial Cleft 2; OFC2
600757	Orofacial Cleft 3; OFC3
608371	Orofacial Cleft 4; OFC4
608874	Orofacial Cleft 5; OFC5 (1 mouse model)
608864	Orofacial Cleft 6, Susceptibility To; OFC6
610361	Orofacial Cleft 9; OFC9
258850	Orofaciodigital Syndrome III; OFD3
311200	Orofaciodigital Syndrome I; OFD1 (2 mouse models)
258860	Orofaciodigital Syndrome IV; OFD4
258865	Orofaciodigital Syndrome IX; OFD9
300484	Orofaciodigital Syndrome Viii; OFD8
608518	Orofaciodigital Syndrome VII; OFD7
277170	Orofaciodigital Syndrome Vi; OFD6
174300	Orofaciodigital Syndrome V; OFD5
612913	Orofaciodigital Syndrome XI; OFD11
165590	Orofaciodigital Syndrome X; OFD10
258900	Orotic Aciduria
143850	Orthostatic Hypotensive Disorder, Streeten Type
604715	Orthostatic Intolerance
603389	Osebold Skeletal Dysplasia/Osteolysis Syndrome
165660	Oslam Syndrome
166350	Osseous Heteroplasia, Progressive; POH
165680	Ossicular Malformations, Familial
602475	Ossification of the Posterior Longitudinal Ligament of Spine; OPLL (1 mouse model)
165670	Ossified Ear Cartilages
259050	Ossified Ear Cartilages with Mental Deficiency, Muscle Wasting, and Bony Changes
165720	Osteoarthritis Susceptibility 1; OS1 (7 mouse models)
140600	Osteoarthritis Susceptibility 2; OS2
607850	Osteoarthritis Susceptibility 3; OS3
610839	Osteoarthritis Susceptibility 4; OS4
612400	Osteoarthritis Susceptibility 5; OS5
612401	Osteoarthritis Susceptibility 6; OS6
604864	Osteoarthritis with Mild Chondrodysplasia
165800	Osteochondritis Dissecans, Short Stature, and Early-Onset Osteoarthritis;
166990	Osteochondrodysplasia, Rhizomelic, with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension (1 mouse model)
259250	Osteodysplasia, Familial, Anderson Type
259270	Osteodysplasty, Precocious, of Danks, Mayne, and Kozlowski
607278	Osteofibrous Dysplasia
259410	Osteogenesis Imperfecta Congenita, Microcephaly, and Cataracts
166200	Osteogenesis Imperfecta, Type I (3 mouse models)
166210	Osteogenesis Imperfecta, Type II (2 mouse models)
259420	Osteogenesis Imperfecta, Type III (3 mouse models)
166220	Osteogenesis Imperfecta, Type IV
259440	Osteogenesis Imperfecta, Type IX; OI9
610682	Osteogenesis Imperfecta, Type VII (1 mouse model)
610915	Osteogenesis Imperfecta, Type VIII (1 mouse model)
613982	Osteogenesis Imperfecta, Type Vi; OI6
610967	Osteogenesis Imperfecta, Type V; OI5 (1 mouse model)
613848	Osteogenesis Imperfecta, Type X
614856	Osteogenesis Imperfecta, Type Xiii; OI13
613849	Osteogenesis Imperfecta, Type Xii; OI12
615066	Osteogenesis Imperfecta, Type Xiv; OI14
610968	Osteogenesis Imperfecta, Type XI, with or without Joint Contractures;
166230	Osteogenesis Imperfecta with Opalescent Teeth, Blue Sclerae and Wormian Bones, but without Fractures
259500	Osteogenic Sarcoma
166250	Osteoglophonic Dysplasia; OGD
259550	Osteoid Osteoma
259610	Osteolysis Syndrome, Recessive
259660	Osteomalacia, Sclerosing, with Cerebral Calcification
603600	Osteoma of Cranial Vault, Familial
259650	Osteoma of Middle Ear
166400	Osteomas of Mandible
166450	Osteomesopyknosis
612852	Osteomyelitis, Sterile Multifocal, with Periostitis and Pustulosis;
300373	Osteopathia Striata with Cranial Sclerosis; OSCS (2 mouse models)
259690	Osteopenia and Sparse Hair (1 mouse model)
600329	Osteopetrosis and Infantile Neuroaxonal Dystrophy
607634	Osteopetrosis, Autosomal Dominant 1; OPTA1
166600	Osteopetrosis, Autosomal Dominant 2; OPTA2
259700	Osteopetrosis, Autosomal Recessive 1; OPTB1 (2 mouse models)
259710	Osteopetrosis, Autosomal Recessive 2; OPTB2
259730	Osteopetrosis, Autosomal Recessive 3; OPTB3 (1 mouse model)
611490	Osteopetrosis, Autosomal Recessive 4; OPTB4 (2 mouse models)
259720	Osteopetrosis, Autosomal Recessive 5; OPTB5 (1 mouse model)
611497	Osteopetrosis, Autosomal Recessive 6; OPTB6
612301	Osteopetrosis, Autosomal Recessive 7; OPTB7
615085	Osteopetrosis, Autosomal Recessive 8; OPTB8
166705	Osteopoikilosis and Dacryocystitis
166710	Osteoporosis (4 mouse models)
601220	Osteoporosis and Oculocutaneous Hypopigmentation Syndrome; OOCH
259750	Osteoporosis, Juvenile
259770	Osteoporosis-Pseudoglioma Syndrome; OPPG (2 mouse models)
166740	Osteosclerosis with Ichthyosis and Fractures
609993	Osteosclerosis with Ichthyosis and Premature Ovarian Failure
603393	Osteosclerotic Chondrodysplasia, Lethal, with Intracellular Inclusions
166760	Otitis Media, Susceptibility to (21 mouse models)
166750	Otodental Dysplasia
166780	Otofaciocervical Syndrome
601976	Otofacioosseous-Gonadal Syndrome
259780	Otoonychoperoneal Syndrome
304120	Otopalatodigital Syndrome, Type II; OPD2 (1 mouse model)
311300	Otopalatodigital Syndrome, Type I; OPD1 (1 mouse model)
166800	Otosclerosis 1; OTSC1
605727	Otosclerosis 2; OTSC2
608244	Otosclerosis 3; OTSC3
611571	Otosclerosis 4; OTSC4
608787	Otosclerosis 5; OTSC5
611572	Otosclerosis 7; OTSC7
612096	Otosclerosis 8; OTSC8
215150	Otospondylomegaepiphyseal Dysplasia; OSMED (1 mouse model)
311350	Ouabain Resistance; OUBR
166900	Ovalocytosis, Hereditary Hemolytic
166910	Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis
167000	Ovarian Cancer (14 mouse models)
607893	Ovarian Cancer, Susceptibility to, 1; OVCAS1
233300	Ovarian Dysgenesis 1; ODG1 (1 mouse model)
300510	Ovarian Dysgenesis 2; ODG2
614324	Ovarian Dysgenesis 3; ODG3
605756	Ovarian Dysgenesis, Hypergonadotropic, with Short Stature and Recurrent Metabolic Acidosis
166970	Ovarian Fibromata
603737	Ovarian Germ Cell Cancer
608115	Ovarian Hyperstimulation Syndrome (1 mouse model)

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