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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
OMIM:601665 Obesity
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: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:257850 Oculodentodigital Dysplasia, Autosomal Recessive
OMIM:164200 Oculodentodigital Dysplasia; ODDD
OMIM:600268 Oculoectodermal Syndrome; OES
OMIM:257910 Oculopalatocerebral Syndrome
OMIM:164300 Oculopharyngeal Muscular Dystrophy; OPMD
OMIM:164310 Oculopharyngodistal Myopathy; OPDM
OMIM:257970 Oculorenocerebellar Syndrome
OMIM:257960 Oculotrichodysplasia; OTD
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
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:258300 Olivopontocerebellar Atrophy II, Autosomal Recessive
OMIM:164700 Olivopontocerebellar Atrophy V; OPCA V
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:164891 Oncogene Yuasa
OMIM:164680 Onychogryposis, Pedal, with Keratosis Plantaris and Coarse Hair
OMIM:258360 Onychotrichodysplasia and Neutropenia
OMIM:615774 Oocyte Maturation Defect 1; OOMD1
OMIM:616780 Oocyte Maturation Defect 2; OOMD2
OMIM:617712 Oocyte Maturation Defect 3; OOMD3
OMIM:617743 Oocyte Maturation Defect 4; OOMD4
OMIM:164900 Ophthalmomandibulomelic Dysplasia
OMIM:311000 Ophthalmoplegia, External, and Myopia; OPEM
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, Type I; GBBB1
OMIM:145410 Opitz Gbbb Syndrome, Type II; GBBB2
OMIM:305450 Opitz-Kaveggia Syndrome; OKS
OMIM:258480 Opsismodysplasia; OPSMD
OMIM:616732 Optic Atrophy 10 with or without Ataxia, Mental Retardation, and Seizures;
OMIM:617302 Optic Atrophy 11; OPA11
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:165510 Optic Atrophy with Negative Electroretinograms
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:610361 Orofacial Cleft 9; OFC9
OMIM:258850 Orofaciodigital Syndrome III; OFD3
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:165590 Orofaciodigital Syndrome X; OFD10
OMIM:617563 Orofaciodigital Syndrome Xvi; OFD16
OMIM:617127 Orofaciodigital Syndrome Xv; OFD15
OMIM:258900 Orotic Aciduria
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: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:613848 Osteogenesis Imperfecta, Type X; OI10
OMIM:616507 Osteogenesis Imperfecta, Type Xvii; OI17
OMIM:616229 Osteogenesis Imperfecta, Type Xvi; OI16
OMIM:615220 Osteogenesis Imperfecta, Type Xv; OI15
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:259660 Osteomalacia, Sclerosing, with Cerebral Calcification
OMIM:603600 Osteoma of Cranial Vault, Familial
OMIM:259650 Osteoma of Middle Ear
OMIM:166400 Osteomas of Mandible
OMIM:166450 Osteomesopyknosis
OMIM:612852 Osteomyelitis, Sterile Multifocal, with Periostitis and Pustulosis;
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: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:166705 Osteopoikilosis and Dacryocystitis
OMIM:166710 Osteoporosis
OMIM:601220 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome; OOCH
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
OMIM:166750 Otodental Dysplasia
OMIM:166780 Otofaciocervical Syndrome 1; OTFCS
OMIM:615560 Otofaciocervical Syndrome 2; 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: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: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: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

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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory