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

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Human Diseases/Syndromes Beginning with "O"

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

OMIM IDHuman Disease
601665 Obesity (60 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)
600268 Oculoectodermal Syndrome; OES
610332 Oculootofacial Dysplasia
257910 Oculopalatocerebral Syndrome (1 mouse models)
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
258040 Oeis Complex
300855 Ogden Syndrome; OGDNS
258100 Oguchi Disease 1
613411 Oguchi Disease 2 (1 mouse models)
249620 Ohdo Syndrome
603736 Ohdo Syndrome, Sbbys Variant; SBBYSS
300895 Ohdo Syndrome, X-Linked; OHDOX
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 models)
258315 Omodysplasia 1; OMOD1
164745 Omodysplasia 2; OMOD2
164750 Omphalocele, Autosomal (1 mouse models)
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
615774 Oocyte Maturation Defect; OOMD
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 models)
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; OPA3
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
615892 Orofacial Cleft 14; OFC14
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 models)
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
615948 Orofaciodigital Syndrome Xiv; OFD14
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 models)
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 models)
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 (3 mouse models)
259420 Osteogenesis Imperfecta, Type III (4 mouse models)
166220 Osteogenesis Imperfecta, Type IV
259440 Osteogenesis Imperfecta, Type IX; OI9
610915 Osteogenesis Imperfecta, Type Viii; OI8 (1 mouse models)
610682 Osteogenesis Imperfecta, Type VII; OI7 (1 mouse models)
613982 Osteogenesis Imperfecta, Type VI; OI6
610967 Osteogenesis Imperfecta, Type V; OI5 (1 mouse models)
613848 Osteogenesis Imperfecta, Type X
614856 Osteogenesis Imperfecta, Type Xiii; OI13
613849 Osteogenesis Imperfecta, Type Xii; OI12
610968 Osteogenesis Imperfecta, Type XI; OI11
615066 Osteogenesis Imperfecta, Type Xiv; OI14
615220 Osteogenesis Imperfecta, Type Xv; OI15
166230 Osteogenesis Imperfecta with Opalescent Teeth, Blue Sclerae and Wormian Bones, but without Fractures
259500 Osteogenic Sarcoma (6 mouse models)
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 models)
600329 Osteopetrosis and Infantile Neuroaxonal Dystrophy
607634 Osteopetrosis, Autosomal Dominant 1; OPTA1
166600 Osteopetrosis, Autosomal Dominant 2; OPTA2 (5 mouse models)
259700 Osteopetrosis, Autosomal Recessive 1; OPTB1 (2 mouse models)
259710 Osteopetrosis, Autosomal Recessive 2; OPTB2
259730 Osteopetrosis, Autosomal Recessive 3; OPTB3 (1 mouse models)
611490 Osteopetrosis, Autosomal Recessive 4; OPTB4 (2 mouse models)
259720 Osteopetrosis, Autosomal Recessive 5; OPTB5 (1 mouse models)
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
615198 Osteosclerotic Metaphyseal Dysplasia; OSMD
166760 Otitis Media, Susceptibility to (22 mouse models)
166750 Otodental Dysplasia
166780 Otofaciocervical Syndrome 1; OFC1
615560 Otofaciocervical Syndrome 2; OFC2
601976 Otofacioosseous-Gonadal Syndrome
259780 Otoonychoperoneal Syndrome
304120 Otopalatodigital Syndrome, Type II; OPD2 (1 mouse models)
311300 Otopalatodigital Syndrome, Type I; OPD1 (1 mouse models)
615589 Otosclerosis 10; OTSC10
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 models)
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 models)
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 models)
185000 Overhydrated Hereditary Stomatocytosis; OHS

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last database update
09/09/2014
MGI 5.19
The Jackson Laboratory