Disease Name Symbol Acronym
O Donnell Pappas Syndrome ODN003
Obesity Due to Congenital Leptin Resistance OBS083
Obesity Due to Melanocortin 4 Receptor Deficiency OBS067
Obesity Due to Sim1 Deficiency OBS060
Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair OBS081 OBAIRH
Obesity, Hyperphagia, and Developmental Delay OBS015 OBHD
Obesity-Colitis-Hypothyroidism-Cardiac Hypertrophy-Developmental Delay Syndrome OBS068
Obesity-Hypoventilation Syndrome OBS037
Obsessive-Compulsive Disorder OBS002 OCD
Obsessive-Compulsive Personality Disorder OBS003 OCPD
Obstructive Hydrocephalus OBS004
Obstructive Jaundice OBS001
Obstructive Nephropathy OBS082 CON
Occipital Encephalocele OCC011
Occipital Hair, White Lock of OCC015
Occipital Horn Syndrome OCC006 OHS
Occipital Lobe Neoplasm OCC003
Occipital Neuralgia OCC008
Occlusion of Gallbladder OCC004
Occlusion Precerebral Artery OCC005
Occult Macular Dystrophy OCC002 OCMD
Occupational Allergic Alveolitis OCC014
Occupational Asthma OCC016
Occupational Dermatitis OCC001
Ochronosis OCH001
Ocular Albinism OCL001 OA
Ocular Albinism with Congenital Sensorineural Deafness OCL062
Ocular Albinism, X-Linked OCL016 OA1
Ocular Cancer OCL009
Ocular Cicatricial Pemphigoid OCL020 OCP
Ocular Dominance OCL052
Ocular Hyperemia OCL004
Ocular Hypertension OCL006
Ocular Hypotension OCL010
Ocular Melanoma OCL022
Ocular Motility Disease OCL011
Ocular Motor Apraxia OCL069 COMA
Ocular Motor Apraxia, Cogan Type OCL054
Ocular Muscular Dystrophy OCL023
Ocular Myopathy with Curare Sensitivity OCL072
Ocular Neuromyotonia OCL024
Ocular Toxoplasmosis OCL025
Ocular Tuberculosis OCL051
Oculo Digital Syndrome OCL028
Oculo Skeletal Renal Syndrome OCL029
Oculoauricular Syndrome OCL048 OCACS
Oculoauriculofrontonasal Syndrome OCL030 OAFNS
Oculo-Cerebral Dysplasia OCL031
Oculocerebral Hypopigmentation Syndrome of Preus OCL071
Oculocerebral Syndrome with Hypopigmentation OCL033
Oculocerebrocutaneous Syndrome OCL034 OCCS
Oculocutaneous Albinism OCL002 OCA
Oculocutaneous Albinism, Type Viii OCL081 OCA8
Oculocutaneous or Ocular Albinism OCL075
Oculodentodigital Dysplasia OCL013 ODDD
Oculodentodigital Dysplasia Dominant OCL037
Oculodentodigital Dysplasia, Autosomal Recessive OCL047 ODDD-AR
Oculodentoosseous Dysplasia Recessive OCL038
Oculoectodermal Syndrome OCL039 OES
Oculoglandular Tularemia OCL007
Oculogyric Crisis OCL066
Oculomaxillofacial Dysostosis OCL040
Oculomedin OCL078 OCLM
Oculomotor Apraxia OCL015
Oculomotor Nerve Paralysis OCL003
Oculomotor-Abducens Synkinesis OCL082 OCABSN
Oculomotor-Levator Synkinesis OCL079 OCLEVS
Oculopalatocerebral Syndrome OCL070
Oculopharyngeal Muscular Dystrophy OCL008 OPMD
Oculopharyngeal Myopathy with Leukoencephalopathy 1 OCL077 OPML1
Oculopharyngodistal Myopathy 1 OCL076 OPDM1
Oculopharyngodistal Myopathy 2 OCL080 OPDM2
Oculorenocerebellar Syndrome OCL043
Oculoskeletodental Syndrome OCL073 OCSKD
Oculotrichodysplasia OCL057 OTD
O'donnell-Luria-Rodan Syndrome ODN024 ODLURO
Odonto Onycho Dysplasia with Alopecia ODN004
Odontochondrodysplasia ODN023 ODCD
Odontoclasia ODN001
Odontogenic Myxoma ODN005
Odontoid Hypoplasia ODN022
Odontoma ODN006
Odontoma-Dysphagia Syndrome ODN020
Odontomicronychial Dysplasia ODN008
Odontoonychodermal Dysplasia ODN009 OODD
Odontotrichoungual-Digital-Palmar Syndrome ODN021
Odor, Male, Women's Choice of ODR001
Oeis Complex OSC001
Oesophagostomiasis OSP001
Ogden Syndrome OGD001 OGDNS
Ogilvie Syndrome OGL001 ACPO
Oguchi Disease OGC005
Oguchi Disease 1 OGC001 CSNBO1
Oguchi Disease 2 OGC002 CSNBO2
Ohdo Syndrome OHD004 BMRS
Ohdo Syndrome, Maat-Kievit-Brunner Type OHD001
Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant OHD002
Ohdo Syndrome, Sbbys Variant OHD005 SBBYSS
Ohdo Syndrome, X-Linked OHD003 OHDOX
Ohtahara Syndrome OHT001
Okihiro Syndrome Due to 20q13 Microdeletion OKH002
Okihiro Syndrome Due to a Point Mutation OKH001
Okt4 Epitope Deficiency OKT001
Okur-Chung Neurodevelopmental Syndrome OKR001 OCNDS
Olecranon Bursitis OLC001
Olfactory Groove Meningioma OLF002
Olfactory Nerve Disease OLF001
Olfactory Nerve Neoplasm OLF004
Olfactory Neural Tumor OLF003
Olfactory Neuroblastoma OLF005
Oligoarticular Juvenile Idiopathic Arthritis OLG020
Oligoasthenoteratozoospermia OLG022 OAT
Oligoastrocytic Tumor OLG023
Oligoastrocytoma OLG006 MOA
Oligocone Trichromacy OLG014
Oligodendroglioma OLG002
Oligodontia-Colorectal Cancer Syndrome OLG005 ODCRCS
Oligohydramnios OLG003
Oligomeganephronia OLG021
Oligosaccharidosis OLG024
Oligospermia OLG001
Oliver Syndrome OLV002
Oliver-Mcfarlane Syndrome OLV004 OMCS
Olivopontocerebellar Atrophy OLV001 OPCA
Olivopontocerebellar Atrophy Deafness OLV003
Olivopontocerebellar Atrophy Ii, Autosomal Recessive OLV006
Olivopontocerebellar Atrophy V OLV005 OPCA V
Olmsted Syndrome 1 OLM003 OLMS1
Olmsted Syndrome 2 OLM004 OLMS2
Olmsted Syndrome, X-Linked OLM002 OLMSX
Omenn Syndrome OMN001 OS
Omodysplasia OMD003
Omodysplasia 1 OMD001 OMOD1
Omodysplasia 2 OMD002 OMOD2
Omphalocele OMP004
Omphalocele, Autosomal OMP009 OMPHA
Omphalocele, Diaphragmatic Hernia, and Radial Ray Defects OMP011
Omphalocele, X-Linked OMP010
Omphalocele-Cleft Palate Syndrome, Lethal OMP008
Omphalomesenteric Cyst OMP003
Omsk Hemorrhagic Fever OMS001 OHF
Onchocerciasis ONC002
Oncocytic Breast Carcinoma ONC001
Oncocytoma ONC007
Oncogene Bmyc ONC005 BMYC
Oncogene Rmyc ONC006 RMYC
Oncogenic Osteomalacia ONC003 TIO
Onychocytic Matricoma ONY004
Onychodystrophy-Anonychia ONY006
Onychogryposis, Pedal, with Keratosis Plantaris and Coarse Hair ONY007
Onychomatricoma ONY005
Onychotrichodysplasia and Neutropenia ONY002
O'nyong'nyong Fever ONY001
Oocyte Maturation Defect 1 OCY003 OOMD1
Oocyte Maturation Defect 10 OCY011 OOMD10
Oocyte Maturation Defect 2 OCY002 OOMD2
Oocyte Maturation Defect 3 OCY004 OOMD3
Oocyte Maturation Defect 4 OCY005 OOMD4
Oocyte Maturation Defect 5 OCY006 OOMD5
Oocyte Maturation Defect 6 OCY007 OOMD6
Oocyte Maturation Defect 7 OCY008 OOMD7
Oocyte Maturation Defect 8 OCY009 OOMD8
Oocyte Maturation Defect 9 OCY010 OOMD9
Open Iniencephaly OPN003
Open-Angle Glaucoma OPN001
Ophn1 Syndrome OPH015
Ophthalmia Neonatorum OPH002
Ophthalmia Nodosa OPH003
Ophthalmomandibulomelic Dysplasia OPH014
Ophthalmomyiasis OPH001
Ophthalmoplegia Totalis with Ptosis and Miosis OPH018
Ophthalmoplegia, External, and Myopia OPH020 OPEM
Ophthalmoplegia, External, with Rib and Vertebral Anomalies OPH021 EORVA
Ophthalmoplegia, Familial Static OPH016
Ophthalmoplegia, Familial Total, with Iris Transillumination OPH017
Ophthalmoplegia, Progressive, with Scrotal Tongue and Mental Deficiency OPH013
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria OPH019
Opiate Dependence OPT003
Opioid Abuse OPD001
Opioid Addiction OPD006
Opioid Dependence 1 OPD004 ODS1
Opisthorchiasis OPS001
Opitz Gbbb Syndrome, Type I OPT051 GBBB1
Opitz Gbbb Syndrome, Type Ii OPT050 GBBB2
Opitz-Gbbb Syndrome OPT048
Opitz-Kaveggia Syndrome OPT054 OKS
Opportunistic Bacterial Infectious Disease OPP001
Opportunistic Mycosis OPP002
Oppositional Defiant Disorder OPP004
Opsismodysplasia OPS002 OPSMD
Opsoclonus-Myoclonus Syndrome OPS006 OMS
Opthalmomandibulomelic Dysplasia OPT018
Optic Atrophy 1 OPT053 OPA1
Optic Atrophy 10 with or Without Ataxia, Mental Retardation, and Seizures OPT062 OPA10
Optic Atrophy 11 OPT064 OPA11
Optic Atrophy 12 OPT080 OPA12
Optic Atrophy 13 with Retinal and Foveal Abnormalities OPT079 OPA13
Optic Atrophy 2 OPT023 OPA2
Optic Atrophy 3, Autosomal Dominant OPT068 OPA3
Optic Atrophy 4 OPT059 OPA4
Optic Atrophy 5 OPT024 OPA5
Optic Atrophy 6 OPT025 OPA6
Optic Atrophy 7 with or Without Auditory Neuropathy OPT074 OPA7
Optic Atrophy 8 OPT060 OPA8
Optic Atrophy 9 OPT065 OPA9
Optic Atrophy with Demyelinating Disease of Cns OPT067
Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy OPT066 DOA+
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant OPT029
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Recessive OPT071
Optic Atrophy-Ataxia-Peripheral Neuropathy-Global Developmental Delay Syndrome OPT078
Optic Atrophy--Spastic Paraplegia Syndrome OPT073
Optic Disc Anomalies with Retinal and/or Macular Dystrophy OPT058 ODRMD
Optic Disc Pit OPT077
Optic Disk Drusen OPT001
Optic Nerve Astrocytoma OPT005
Optic Nerve Disease OPT006
Optic Nerve Glioma OPT007
Optic Nerve Hypoplasia, Bilateral OPT070 BONH
Optic Nerve Neoplasm OPT008
Optic Nerve Sheath Meningioma OPT002
Optic Neuritis OPT009
Optic Neuritis with Anti-Mog Antibodies OPT081
Optic Papillitis OPT010
Optic Pathway Glioma OPT032
Opticocochleodentate Degeneration OPT072
Oral and Digital Anomalies with Ichthyosis ORL024
Oral Cancer ORL011
Oral Candidiasis ORL005
Oral Cavity Cancer ORL007
Oral Cavity Carcinoma in Situ ORL001
Oral Erosive Lichen ORL022
Oral Hairy Leukoplakia ORL019
Oral Leukoedema ORL002
Oral Leukoplakia ORL012
Oral Lichen Planus ORL013
Oral Mucosa Leukoplakia ORL006
Oral Sensibility, Disturbance of ORL026
Oral Squamous Cell Carcinoma ORL015
Oral Submucous Fibrosis ORL004 OSMF
Oral Tuberculosis ORL003
Oral-Facial-Digital Syndrome with Short Stature and Brachymesophalangy ORL028 OFD18
Orange Allergy ORN009
Orbit Alveolar Rhabdomyosarcoma ORB001
Orbit Embryonal Rhabdomyosarcoma ORB002
Orbit Lymphoma ORB009
Orbit Rhabdomyosarcoma ORB011
Orbital Cancer ORB012
Orbital Cellulitis ORB006
Orbital Cyst ORB007
Orbital Disease ORB013 ORBIT
Orbital Granuloma ORB010
Orbital Leiomyoma ORB018
Orbital Lymphangioma ORB014
Orbital Lymphoma ORB020
Orbital Margin, Hypoplasia of ORB019
Orbital Osteomyelitis ORB004
Orbital Periostitis ORB005
Orbital Plasma Cell Granuloma ORB008
Orbital Tenonitis ORB003
Orbital Varix ORB016
Orchitis ORC001
Organic Acidemia ORG002
Organic Mood Syndrome ORG003
Orgasm-Induced Seizures ORG008
Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to ORN008 OTCD
Ornithinemia ORN004
Ornithosis ORN001
Oroacral Syndrome, Verloes-Koulischer Type ORC002
Orofacial Cleft ORF002
Orofacial Cleft 1 ORF048 OFC1
Orofacial Cleft 10 ORF028 OFC10
Orofacial Cleft 11 ORF027 OFC11
Orofacial Cleft 12 ORF020 OFC12
Orofacial Cleft 13 ORF029 OFC13
Orofacial Cleft 14 ORF031 OFC14
Orofacial Cleft 15 ORF047 OFC15
Orofacial Cleft 2 ORF050 OFC2
Orofacial Cleft 3 ORF049 OFC3
Orofacial Cleft 4 ORF023 OFC4
Orofacial Cleft 5 ORF014 OFC5
Orofacial Cleft 6 ORF025 OFC6
Orofacial Cleft 8 ORF016 OFC8
Orofacial Cleft 9 ORF024 OFC9
Orofacial Clefting Syndrome ORF053
Orofacial Granulomatosis ORF044
Orofaciodigital Syndrome ORF001 OFD
Orofaciodigital Syndrome 12 ORF005 OFD12
Orofaciodigital Syndrome 13 ORF006 OFD13
Orofaciodigital Syndrome I ORF037 OFD1
Orofaciodigital Syndrome Iii ORF038 OFD3
Orofaciodigital Syndrome Iv ORF035 OFD4
Orofaciodigital Syndrome Ix ORF043 OFD9
Orofaciodigital Syndrome V ORF033 OFD5
Orofaciodigital Syndrome Vi ORF034 OFD6
Orofaciodigital Syndrome Vii ORF039 OFD7
Orofaciodigital Syndrome Viii ORF040 OFD8
Orofaciodigital Syndrome X ORF041 OFD10
Orofaciodigital Syndrome Xi ORF042 OFD11
Orofaciodigital Syndrome Xiv ORF036 OFD14
Orofaciodigital Syndrome Xv ORF045 OFD15
Orofaciodigital Syndrome Xvi ORF046 OFD16
Orofaciodigital Syndrome Xvii ORF051 OFD17
Orofaciodigital Syndrome Xviii ORF052 OFD18
Oromandibular Dystonia ORM002
Oromandibular-Limb Anomalies Syndrome ORM003
Oro-Mandibular-Limb Hypogenesis Syndrome ORM001
Oropharyngeal Anthrax ORP001
Oropharynx Cancer ORP003
Oropouche Fever ORP002
Orotic Aciduria ORT008 ORAC1
Orthostatic Hypotension 1 ORT011 ORTHYP1
Orthostatic Hypotension 2 ORT012 ORTHYP2
Orthostatic Hypotensive Disorder, Streeten Type ORT010 OHDS
Orthostatic Intolerance ORT004 OI
Orthostatic Proteinuria ORT001
Osebold Skeletal Dysplasia/osteolysis Syndrome OSB002
Osebold-Remondini Syndrome OSB001 BDA6
Osgood-Schlatter's Disease OSG001
Oslam Syndrome OSL001
Osmotic Diarrhea OSM001
Osseous Heteroplasia, Progressive OSS012 POH
Ossicular Malformations, Familial OSS006
Ossification Anomalies-Psychomotor Developmental Delay Syndrome OSS015
Ossification of the Posterior Longitudinal Ligament of Spine OSS014 OPLL
Ossified Ear Cartilages OSS016
Ossifying Fibroma OSS001
Ossifying Fibromyxoid Tumor OSS002
Osteitis Fibrosa OST004
Osteoarthritis OST012 OA
Osteoarthritis with Mild Chondrodysplasia OST062 OSCDP
Osteoblastoma OST006
Osteochondritis Dissecans OST009 OCD
Osteochondrodysplasia, Brachydactyly, and Overlapping Malformed Digits OST172 OCBMD
Osteochondrodysplasia, Complex Lethal, Symoens-Barnes-Gistelinck Type OST153 OCLSBG
Osteochondrodysplasia, Rhizomelic, with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension OST157
Osteochondrodysplatic Nanism-Deafness-Retinitis Pigmentosa Syndrome OST145
Osteochondroma OST028
Osteochondrosis OST016
Osteochondrosis of Genetic Origin OST174
Osteochondrosis of the Metatarsal Bone OST177
Osteoclastic Giant Cell Tumor of Pancreas OST141
Osteoclast-Like Giant Cell Neoplasm of the Pancreas OST010
Osteodysplasia, Familial, Anderson Type OST150
Osteodysplasty, Precocious, of Danks, Mayne, and Kozlowski OST158
Osteofibrous Dysplasia OST032 OSFD
Osteogenesis Imperfecta Congenita, Microcephaly, and Cataracts OST148
Osteogenesis Imperfecta with Opalescent Teeth, Blue Sclerae and Wormian Bones, but Without Fractures OST154
Osteogenesis Imperfecta, Type I OST135 OI1
Osteogenesis Imperfecta, Type Ii OST080 OI2
Osteogenesis Imperfecta, Type Iii OST122 OI3
Osteogenesis Imperfecta, Type Iv OST121 OI4
Osteogenesis Imperfecta, Type Ix OST130 OI9
Osteogenesis Imperfecta, Type V OST124 OI5
Osteogenesis Imperfecta, Type Vi OST132 OI6
Osteogenesis Imperfecta, Type Vii OST119 OI7
Osteogenesis Imperfecta, Type Viii OST118 OI8
Osteogenesis Imperfecta, Type X OST127 OI10
Osteogenesis Imperfecta, Type Xi OST133 OI11
Osteogenesis Imperfecta, Type Xii OST128 OI12
Osteogenesis Imperfecta, Type Xiii OST123 OI13
Osteogenesis Imperfecta, Type Xiv OST109 OI14
Osteogenesis Imperfecta, Type Xix OST170 OI19
Osteogenesis Imperfecta, Type Xv OST110 OI15
Osteogenesis Imperfecta, Type Xvi OST139 OI16
Osteogenesis Imperfecta, Type Xvii OST138 OI17
Osteogenesis Imperfecta, Type Xviii OST169 OI18
Osteogenesis Imperfecta, Type Xx OST176 OI20
Osteogenesis Imperfecta, Type Xxi OST178 OI21
Osteogenesis Imperfecta-Retinopathy-Seizures-Intellectual Disability Syndrome OST142
Osteogenic Sarcoma OST159 OSRC
Osteoglophonic Dysplasia OST044 OGD
Osteoid Osteoma OST160
Osteolysis Syndrome, Recessive OST149
Osteoma of Cranial Vault, Familial OST166
Osteoma of Middle Ear OST161
Osteomalacia OST011
Osteomalacia, Sclerosing, with Cerebral Calcification OST162
Osteomas of Mandible OST155
Osteomesopyknosis OST117
Osteomyelitis OST017
Osteomyelitis, Sterile Multifocal, with Periostitis and Pustulosis OST167 OMPP
Osteonecrosis OST003
Osteonecrosis of Genetic Origin OST175
Osteonecrosis of the Jaw OST115
Osteopathia Striata with Cranial Sclerosis OST022 OSCS
Osteopathia Striata with Pigmentary Dermopathy Including White Forelock OST046
Osteopenia and Sparse Hair OST047
Osteopenia-Myopia-Hearing Loss-Intellectual Disability-Facial Dysmorphism Syndrome OST146
Osteopetrosis OST001
Osteopetrosis and Infantile Neuroaxonal Dystrophy OST048
Osteopetrosis, Autosomal Dominant 1 OST125 OPTA1
Osteopetrosis, Autosomal Dominant 2 OST131 OPTA2
Osteopetrosis, Autosomal Dominant 3 OST171 OPTA3
Osteopetrosis, Autosomal Recessive 1 OST126 OPTB1
Osteopetrosis, Autosomal Recessive 2 OST129 OPTB2
Osteopetrosis, Autosomal Recessive 3 OST163 OPTB3
Osteopetrosis, Autosomal Recessive 4 OST137 OPTB4
Osteopetrosis, Autosomal Recessive 5 OST120 OPTB5
Osteopetrosis, Autosomal Recessive 6 OST134 OPTB6
Osteopetrosis, Autosomal Recessive 7 OST136 OPTB7
Osteopetrosis, Autosomal Recessive 8 OST106 OPTB8
Osteopoikilosis OST014
Osteopoikilosis and Dacryocystitis OST058
Osteoporosis OST002 OSTEOP
Osteoporosis and Oculocutaneous Hypopigmentation Syndrome OST151 OOCH
Osteoporosis, Juvenile OST164 IJO
Osteoporosis-Macrocephaly-Blindness-Joint Hyperlaxity Syndrome OST144
Osteoporosis-Pseudoglioma Syndrome OST024 OPPG
Osteoradionecrosis of the Mandible OST173
Osteosarcoma Arising in Bone Paget's Disease OST013
Osteosclerosis with Ichthyosis and Fractures OST156
Osteosclerosis with Ichthyosis and Premature Ovarian Failure OST061
Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome OST114
Osteosclerotic Chondrodysplasia, Lethal, with Intracellular Inclusions OST165
Osteosclerotic Metaphyseal Dysplasia OST168 OSMD
Osteosclerotic Myeloma OST008
Ostertagiasis OST007
O'sullivan-Mcleod Syndrome OSL002
Other Acquired Skin Disease OTH020
Other Dermis Disorder OTH022
Other Epidermal Disorder OTH023
Other Genetic Dermis Disorder OTH018
Other Genetic Epidermal Disease OTH024
Other Immunodeficiency Syndrome with Predominantly Antibody Defects OTH016
Other Immunodeficiency Syndromes Due to Defects in Innate Immunity OTH017
Other Metabolic Disease OTH021
Other Metabolic Disease with Epilepsy OTH015
Other Metabolic Disease with Skin Involvement OTH019
Other Rare Diabetes Mellitus OTH013
Other Syndrome with a Central Nervous System Malformation As a Major Feature OTH026
Other Syndrome with Lissencephaly As a Major Feature OTH025
Otitis Externa OTT001
Otitis Media OTT002 OMS
Otodental Dysplasia OTD001 OOD
Otofaciocervical Syndrome 1 OTF004 OTFCS
Otofaciocervical Syndrome 2 OTF003 OTFCS2
Otofacioosseous-Gonadal Syndrome OTF005
Otof-Related Deafness OTF001 DFNB9
Otomandibular Dysplasia OTM002
Otomandibular Dysplasia Associated with Monogenic Syndromes OTM003
Otomycosis OTM001
Otoonychoperoneal Syndrome OTN001
Oto-Palatal-Digital Syndrome OTP003
Otopalatodigital Syndrome Spectrum Disorder OTP008 OPSD
Otopalatodigital Syndrome, Type I OTP006 OPD1
Otopalatodigital Syndrome, Type Ii OTP007 OPD2
Otosalpingitis OTS003
Otosclerosis OTS001
Otosclerosis 1 OTS005 OTSC1
Otosclerosis 10 OTS012 OTSC10
Otosclerosis 2 OTS006 OTSC2
Otosclerosis 3 OTS007 OTSC3
Otosclerosis 4 OTS008 OTSC4
Otosclerosis 5 OTS009 OTSC5
Otosclerosis 7 OTS010 OTSC7
Otosclerosis 8 OTS011 OTSC8
Otosclerosis, Familial OTS004
Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant OTS014 OSMEDA
Otospondylomegaepiphyseal Dysplasia, Autosomal Recessive OTS013 OSMEDB
Ouabain Resistance OBN001 OUBR
Outlet Dysfunction Constipation OTL001
Ouvrier Billson Syndrome OVR067
Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis OVL006
Ovalocytosis, Southeast Asian OVL001 SAO
Ovarian Angiosarcoma OVR003
Ovarian Benign Neoplasm OVR041
Ovarian Brenner Tumor OVR010
Ovarian Cancer OVR042 OC
Ovarian Cancer 1 OVR114 OVCAS1
Ovarian Carcinosarcoma OVR044
Ovarian Clear Cell Adenocarcinoma OVR034
Ovarian Clear Cell Adenofibroma OVR045
Ovarian Clear Cell Carcinoma OVR106
Ovarian Clear Cell Cystadenocarcinoma OVR040
Ovarian Clear Cell Cystadenofibroma OVR014
Ovarian Clear Cell Malignant Adenofibroma OVR018
Ovarian Cyst OVR046
Ovarian Cystadenocarcinoma OVR047
Ovarian Cystadenoma OVR048
Ovarian Cystic Teratoma OVR017
Ovarian Disease OVR049
Ovarian Dysgenesis 1 OVR075 ODG1
Ovarian Dysgenesis 2 OVR076 ODG2
Ovarian Dysgenesis 3 OVR102 ODG3
Ovarian Dysgenesis 4 OVR107 ODG4
Ovarian Dysgenesis 5 OVR115 ODG5
Ovarian Dysgenesis 6 OVR118 ODG6
Ovarian Dysgenesis 7 OVR119 ODG7
Ovarian Dysgenesis 8 OVR120 ODG8
Ovarian Dysgenesis, Hypergonadotropic, with Short Stature and Recurrent Metabolic Acidosis OVR113
Ovarian Embryonal Carcinoma OVR050
Ovarian Endodermal Sinus Tumor OVR051
Ovarian Endometrial Cancer OVR103
Ovarian Endometrioid Adenofibroma OVR052
Ovarian Endometrioid Cystadenofibroma OVR036
Ovarian Endometrioid Cystadenoma OVR007
Ovarian Endometrioid Malignant Adenofibroma OVR030
Ovarian Endometrioid Stromal Sarcoma OVR016
Ovarian Epithelial Cancer OVR094 EOC
Ovarian Fetiform Teratoma OVR038
Ovarian Fibroma OVR098
Ovarian Fibromata OVR111
Ovarian Fibrothecoma OVR097
Ovarian Germ Cell Cancer OVR112 MOGCT
Ovarian Germ Cell Teratoma OVR109
Ovarian Gonadoblastoma OVR009
Ovarian Hyperstimulation Syndrome OVR029 OHSS
Ovarian Insufficiency, Familial OVR071
Ovarian Large-Cell Neuroendocrine Carcinoma OVR005
Ovarian Low Malignant Potential Tumor OVR072
Ovarian Lymphoma OVR021
Ovarian Malignant Mesothelioma OVR019
Ovarian Melanoma OVR104
Ovarian Mesodermal Adenosarcoma OVR039
Ovarian Mixed Germ Cell Neoplasm OVR015
Ovarian Mucinous Adenocarcinoma OVR011
Ovarian Mucinous Adenofibroma OVR053
Ovarian Mucinous Cystadenocarcinoma OVR013
Ovarian Mucinous Cystadenofibroma OVR008
Ovarian Mucinous Malignant Adenofibroma OVR025
Ovarian Mucinous Neoplasm OVR054
Ovarian Papillary Cystadenoma OVR031
Ovarian Papillary Neoplasm OVR055
Ovarian Primitive Germ Cell Tumor OVR056
Ovarian Remnant Syndrome OVR073
Ovarian Seromucinous Carcinoma OVR123
Ovarian Serous Adenofibroma OVR057
Ovarian Serous Carcinoma OVR105
Ovarian Serous Cystadenocarcinoma OVR012
Ovarian Serous Cystadenofibroma OVR002
Ovarian Sex Cord-Stromal Benign Neoplasm OVR122
Ovarian Sex-Cord Stromal Tumor OVR121
Ovarian Small Cell Carcinoma OVR058 SCCO
Ovarian Solid Teratoma OVR037
Ovarian Squamous Cell Carcinoma OVR027
Ovarian Squamous Cell Neoplasm OVR028
Ovarian Stromal Hyperthecosis OVR001
Ovarian Surface Papilloma OVR032
Ovarian Wilms' Cancer OVR020
Ovary Adenocarcinoma OVR059
Ovary Epithelial Cancer OVR060
Ovary Leiomyosarcoma OVR035
Ovary Neuroendocrine Neoplasm OVR004
Ovary Papillary Carcinoma OVR033
Ovary Rhabdomyosarcoma OVR023
Ovary Sarcoma OVR061
Ovary Serous Adenocarcinoma OVR062
Ovary Transitional Cell Carcinoma OVR026
Overgrowth or Tall Stature Syndrome with Skeletal Involvement OVR126
Overgrowth Syndrome OVR082
Overgrowth Syndrome with 2q37 Translocation OVR117
Overgrowth/obesity Syndrome OVR124
Overgrowth-Macrocephaly-Facial Dysmorphism Syndrome OVR110
Overhydrated Hereditary Stomatocytosis OVR093 OHST
Overlap Myositis OVR096
Overlapping Connective Tissue Disease OVR125
Overnutrition OVR063
Overuse Syndrome OVR077
Oxirane Allergy OXR001
Oxyphilic Endometrial Endometrioid Adenocarcinoma OXY001
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