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
|