Disease Name Symbol Acronym
O Donnell Pappas Syndrome ODN003
Obesity Due to Congenital Leptin Deficiency OBS050 LEPD
Obesity Due to Congenital Leptin Resistance OBS083
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, Hyperphagia, and Severe Developmental Delay Due Totrkb Gene Deficiency OBS052
Obesity-Colitis-Hypothyroidism-Cardiac Hypertrophy-Developmental Delay Syndrome OBS068
Obesity-Hypoventilation Syndrome OBS037
Obsessive-Compulsive Disorder OBS002 OCD
Obsessive-Compulsive Personality Disorder OBS003 OCPD
Obsolete: Abnormal Eye Movements OBS753
Obsolete: Abnormal Origin or Aberrant Course of Coronary Artery OBS615
Obsolete: Acan-Related Skeletal Dysplasia OBS494
Obsolete: Acenocoumarol Toxicity OBS313
Obsolete: Acheiria, Bilateral OBS438
Obsolete: Acheiria, Unilateral OBS439
Obsolete: Acquired Amyloid Myopathy OBS243
Obsolete: Acquired Metabolic Neuropathy OBS235
Obsolete: Acquired Rod-Body Myopathy OBS242
Obsolete: Acromesomelic Dysplasia, Brahimi-Bacha Type OBS115
Obsolete: Acth-Independent Cushing Syndrome Due to Bilateral Adrenocortical Hyperplasia OBS103
Obsolete: Acute Cutaneous Lupus Erythematosus OBS089
Obsolete: Adactyly of Foot OBS493
Obsolete: Adactyly of Foot, Bilateral OBS447
Obsolete: Adactyly of Foot, Unilateral OBS444
Obsolete: Adactyly of Hand OBS386
Obsolete: Adult Chronic Recurrent Multifocal Osteomyelitis OBS641
Obsolete: Adult-Onset Sapho Syndrome OBS371
Obsolete: Amelia of Lower Limb, Bilateral OBS398
Obsolete: Amelia of Lower Limb, Unilateral OBS399
Obsolete: Amelia of Upper Limb, Bilateral OBS409
Obsolete: Amelia of Upper Limb, Unilateral OBS408
Obsolete: Amitriptyline Toxicity OBS311
Obsolete: Amniotic Bands OBS123
Obsolete: Anemia Due to Adenosine Triphosphatase Deficiency OBS267
Obsolete: Aniridia OBS424
Obsolete: Anomaly of the Secretory and Excretory Apparatus of the Lacrimal System OBS671
Obsolete: Anophthalmia-Esophageal-Genital Syndrome Syndrome OBS835
Obsolete: Antipsychotics Toxicity OBS312
Obsolete: Aortopulmonary Coronary Arterial Course OBS645
Obsolete: Apodia, Bilateral OBS440
Obsolete: Apodia, Unilateral OBS441
Obsolete: Argyrophilic Grain Disease OBS602
Obsolete: Arterial Hypertension Due to Renal Artery Stenosis Secondary to Vasculitis OBS604
Obsolete: Arthrogryposis Due to Muscular Dystrophy OBS094
Obsolete: Arthrogryposis-Epileptic Seizures-Migrational Brain Disorder Syndrome OBS130
Obsolete: Aseptic Osteitis OBS527
Obsolete: Atlantoaxial Subluxation OBS656
Obsolete: Atorvastatin Toxicity OBS306
Obsolete: Atrichia-Mental and Growth Delay Syndrome OBS133
Obsolete: Atrioventricular Discordance OBS729
Obsolete: Atypical Teratoid/rhabdoid Tumor OBS168
Obsolete: Auriculoocular Anomalies-Cleft Lip Syndrome OBS523
Obsolete: Autoimmune Enteropathy Type 2 OBS811
Obsolete: Autoimmune Enteropathy Type 3 OBS809
Obsolete: Autoimmune Neurological Channelopathy Due to a P/q-Type Voltage Gated Calcium Channel Defect OBS757
Obsolete: Autoimmune Neurological Channelopathy Due to a Potassium Channel Defect OBS758
Obsolete: Autoimmune Neurological Channelopathy Due to an Acetylcholine Receptor Subunits Defect OBS759
Obsolete: Autosomal Dominant Childhood-Onset Cortical Cataract OBS431
Obsolete: Autosomal Dominant Focal Dystonia, Dyt7 Type OBS634 DYT7
Obsolete: Autosomal Dominant Optic Atrophy and Late-Onset Deafness OBS176
Obsolete: Autosomal Dominant Spastic Paraplegia Type 9 OBS830 SPG9
Obsolete: Autosomal Dominant Spinocerebellar Ataxia Due to a Channelopathy OBS594
Obsolete: Autosomal Dominant Spinocerebellar Ataxia Due to a Point Mutation OBS598
Obsolete: Autosomal Dominant Spinocerebellar Ataxia Due to a Polyglutamine Anomaly OBS593
Obsolete: Autosomal Dominant Spinocerebellar Ataxia Due to Repeat Expansions That Do Not Encode Polyglutamine OBS599
Obsolete: Autosomal Dominant Trichoodontoonychodysplasia-Syndactyly OBS211
Obsolete: Autosomal Recessive Childhood-Onset Cortical Cataract OBS262
Obsolete: Autosomal Recessive Hyper-Ige Syndrome OBS092
Obsolete: Autosomal Recessive Limb-Girdle Muscular Dystrophy with Cerebellar Involvement OBS382
Obsolete: Autosomal Recessive Optic Atrophy OBS708
Obsolete: Autosomal Recessive Optic Atrophy, Opa6 Type OBS670
Obsolete: Autosomal Recessive Optic Atrophy, Opa9 Type OBS495
Obsolete: Autosomal Recessive Syndromic Optic Atrophy OBS706
Obsolete: Ayme-Gripp Syndrome OBS521
Obsolete: Azathioprine Dose Selection in the Treatment of Crohn Disease, Leukemia and in Transplantation OBS293
Obsolete: Azathioprine Toxicity OBS307
Obsolete: Benign Exophthalmos Syndrome OBS524 BES
Obsolete: Benign Tumor of Palpebral Epidermis OBS698
Obsolete: Binswanger Disease OBS102
Obsolete: Blaichman Syndrome OBS126
Obsolete: Blepharophimosis-Radioulnar Synostosis Syndrome OBS127
Obsolete: Blepharoptosis-Cleft Palate-Ectrodactyly-Dental Anomalies Syndrome OBS252
Obsolete: Bone Disease with Increased Bone Density and Metaphyseal or Diaphyseal Involvement OBS621
Obsolete: Bone Dysplasia, Azouz Type OBS237
Obsolete: Bowed Tibiae-Radial Anomalies-Osteopenia-Fractures Syndrome OBS250
Obsolete: Brachydactyly OBS387
Obsolete: Brachydactyly Group OBS622
Obsolete: Brachydactyly of Fingers OBS413
Obsolete: Brachydactyly of Fingers, Bilateral OBS452
Obsolete: Brachydactyly of Fingers, Unilateral OBS451
Obsolete: Brachydactyly of Toes OBS417
Obsolete: Brachydactyly of Toes, Bilateral OBS454
Obsolete: Brachydactyly of Toes, Unilateral OBS453
Obsolete: Brain Stem Tumor OBS537
Obsolete: Bulbar Conjunctival Dermoid or Conjunctival Dermolipoma OBS728
Obsolete: Bullous Systemic Lupus Erythematosus OBS541 BSLE
Obsolete: Canthal Anomaly OBS701
Obsolete: Capecitabine Toxicity OBS304
Obsolete: Carbamazepine Toxicity OBS305
Obsolete: Carbutamide Toxicity OBS309
Obsolete: Cardiac Disease with Cataract OBS717
Obsolete: Cardioskeletal Syndrome OBS730
Obsolete: Cataract, Hutterite Type OBS667
Obsolete: Central Polydactyly of Fingers, Bilateral OBS475
Obsolete: Central Polydactyly of Fingers, Unilateral OBS468
Obsolete: Central Polydactyly of Toes OBS410
Obsolete: Central Polydactyly of Toes, Bilateral OBS476
Obsolete: Central Polydactyly of Toes, Unilateral OBS477
Obsolete: Cerebral Disease with Cataract OBS719
Obsolete: Cerebrorenodigital Syndrome OBS137
Obsolete: Cervical Dystonia OBS633
Obsolete: Cervicofacial Lymphatic Malformation OBS136
Obsolete: Channelopathy OBS151
Obsolete: Channelopathy Due to a Calcium-Activated Potassium Channel Defect OBS582
Obsolete: Channelopathy Due to a Cardiac Muscle Sarcoplasmic Reticulum Calcium Release Channel Defect OBS588
Obsolete: Channelopathy Due to a Neuronal Acetylcholine Receptor Defect OBS576
Obsolete: Channelopathy Due to a Neuronal Glycine Receptor Defect OBS573
Obsolete: Channelopathy Due to a Neuronal Kidney Gaba Receptor Defect OBS574
Obsolete: Channelopathy Due to a Skeletal Muscle Acetylcholine Receptor Defect OBS575
Obsolete: Channelopathy Due to a Skeletal Muscle Sarcoplasmic Reticulum Calcium Release Channel Defect OBS585
Obsolete: Channelopathy Due to a Transient Receptor Potential Channel Defect OBS580
Obsolete: Channelopathy Due to a Voltage-Gated Calcium Channel Defect OBS584
Obsolete: Channelopathy Due to a Voltage-Gated Potassium Channel Defect OBS577
Obsolete: Channelopathy Due to a Voltage-Gated Sodium Channel Defect OBS581
Obsolete: Channelopathy Due to an Epithelial Sodium Channel Defect OBS586
Obsolete: Channelopathy Due to an Inwardly Rectifying Potassium Channel Defect OBS578
Obsolete: Channelopathy Due to Cyclic Nucleotide-Gated Ion Channels OBS579
Obsolete: Chondrodysplasia Punctata, Sheffield Type OBS565
Obsolete: Chondrodysplastic Malformation Syndrome OBS120
Obsolete: Choristoma OBS560
Obsolete: Choroideremia-Hypopituitarism Syndrome OBS258
Obsolete: Chronic Muscular Fatigue and/or Chronic Muscle Pain OBS238
Obsolete: Cinca Syndrome with Nlrp3 Mutations OBS631
Obsolete: Cinca Syndrome Without Nlrp3 Mutations OBS632
Obsolete: Circumscribed Lymphatic Malformation OBS265
Obsolete: Cisatracurium Toxicity OBS310
Obsolete: Classic Seminoma OBS843
Obsolete: Clomipramine Toxicity OBS308
Obsolete: Cobblestone Lissencephaly Type a OBS378
Obsolete: Cobblestone Lissencephaly Type B OBS380
Obsolete: Cobblestone Lissencephaly Type C OBS379
Obsolete: Collagenous Colitis OBS538
Obsolete: Colobomatous and Areolar Dystrophy OBS712
Obsolete: Combined Hyperlipidemia OBS529
Obsolete: Common Variable Immunodeficiency Due to an Intrinsic B Cell Defect OBS530
Obsolete: Common Variable Immunodeficiency Due to an Intrinsic T Cell Defect OBS846
Obsolete: Common Variable Immunodeficiency Due to Tnfr Deficiency OBS105
Obsolete: Common Variable Immunodeficiency Without Known Genetic Defect OBS273
Obsolete: Congenital Absence of Both Forearm and Hand, Bilateral OBS434
Obsolete: Congenital Absence of Both Forearm and Hand, Unilateral OBS435
Obsolete: Congenital Absence of Both Lower Leg and Foot, Bilateral OBS436
Obsolete: Congenital Absence of Both Lower Leg and Foot, Unilateral OBS437
Obsolete: Congenital Absence of the Eyebrow/eyelashes OBS682
Obsolete: Congenital Absence of Thigh and Lower Leg with Foot Present, Bilateral OBS432
Obsolete: Congenital Absence of Thigh and Lower Leg with Foot Present, Unilateral OBS433
Obsolete: Congenital Absence of Upper Arm and Forearm with Hand Present, Bilateral OBS396
Obsolete: Congenital Absence of Upper Arm and Forearm with Hand Present, Unilateral OBS397
Obsolete: Congenital Absence/hypoplasia of Fingers Excluding Thumb OBS416
Obsolete: Congenital Absence/hypoplasia of Fingers Excluding Thumb, Bilateral OBS445
Obsolete: Congenital Absence/hypoplasia of Thumb, Bilateral OBS442
Obsolete: Congenital Absence/hypoplasia of Thumb, Unilateral OBS443
Obsolete: Congenital Adrenal Hypoplasia of Maternal Cause OBS607
Obsolete: Congenital Blindness Due to Retinal Non-Attachment OBS485
Obsolete: Congenital Cataract, Volkmann Type OBS668
Obsolete: Congenital Cataract-Ichthyosis Syndrome OBS140
Obsolete: Congenital Entropion OBS699
Obsolete: Congenital Hydromyelia OBS205
Obsolete: Congenital Ichthyosis with Trichothiodystrophy OBS422
Obsolete: Congenital Liver Hemangioma OBS277
Obsolete: Congenital Muscular Dystrophy Due to Extracellular Matrix Protein Anomaly OBS797
Obsolete: Congenital Muscular Dystrophy Due to Glycosyltransferase Anomaly OBS798
Obsolete: Congenital Muscular Dystrophy Due to Proteins of the Endoplasmic Reticulum Anomaly OBS799
Obsolete: Congenital Muscular Dystrophy-Muscle Hypertrophy-Severe Intellectual Disability Syndrome OBS369
Obsolete: Congenital Myopathy with Central Nuclei OBS099
Obsolete: Congenital Myopathy with Fiber Size Variation OBS100
Obsolete: Congenital Myopathy with Protein Accumulation OBS101
Obsolete: Congenital Myopathy with Vacuoles OBS098
Obsolete: Congenital Nasal Pyriform Aperture Stenosis with Holoprosencephaly OBS090
Obsolete: Congenital Patella Dislocation, Bilateral OBS483
Obsolete: Congenital Patella Dislocation, Unilateral OBS484
Obsolete: Congenital Primary Lymphedema OBS104
Obsolete: Congenital Upper Palpebral Retraction OBS695
Obsolete: Congenital Vascular Bone Syndrome with Limb Overgrowth OBS275
Obsolete: Congenital Vascular Bone Syndrome with Limb Shortening OBS276
Obsolete: Congenital Vitreoretinal Dysplasia OBS709
Obsolete: Conjunctival Hemangioma or Hemolymphangioma OBS675
Obsolete: Conjunctival Lymphangiectasia OBS673
Obsolete: Conjunctival Telangiectasia OBS672
Obsolete: Conjunctival Tumor OBS726
Obsolete: Conjunctival Vascular Anomaly OBS674
Obsolete: Connective Tissue Disease with Eye Involvement OBS744
Obsolete: Coppock-Like Cataract OBS669
Obsolete: Corneoiridogoniodysgenesis OBS720
Obsolete: Coronary Artery Intramyocardial Course OBS644
Obsolete: Cortada-Koussef-Matsumoto Syndrome OBS147
Obsolete: Corticobasal Degeneration OBS510
Obsolete: Cowpox Infection OBS492
Obsolete: Cranioacrofacial Syndrome OBS142
Obsolete: Craniofacial Dysostosis-Arthrogryposis-Progeroid Appearance Syndrome OBS244
Obsolete: Craniofaciocervical Osteoglyphic Dysplasia OBS156
Obsolete: Craniosynostosis Syndrome or Cranial Ossification Disease OBS623
Obsolete: Craniosynostosis-Cataract Syndrome OBS247
Obsolete: Craniosynostosis-Radial Aplasia, Imaizumi Type OBS230
Obsolete: Craniosynostosis-Synostoses-Hypertensive Nephropathy Syndrome OBS153
Obsolete: Cys-Loop Receptor Channelopathy OBS572
Obsolete: Cystic Malformation of the Posterior Fossa OBS802
Obsolete: Ddx59-Related Orofaciodigital Syndrome OBS375
Obsolete: Deafness-Peripheral Neuropathy-Arterial Disease Syndrome OBS221
Obsolete: Deafness-White Hair-Contractures-Papillomas Syndrome OBS217
Obsolete: Deletion 20p OBS114
Obsolete: Deletion 4q OBS113
Obsolete: Dennis-Cohen Syndrome OBS145
Obsolete: Developmental Delay-Deafness Syndrome, Hildebrand Type OBS087
Obsolete: Diabetes Associated to Exocrine Pancreas Neoplasia OBS600
Obsolete: Disease Predisposing to Age-Related Macular Degeneration OBS711
Obsolete: Disease with Isotype or Light Chain Deficiencies with Normal Numbers of B Cells OBS817
Obsolete: Disease with Potential Neoplastic Degeneration Associated with Ocular Features OBS747
Obsolete: Disease with Severe Reduction in All Serum Immunoglobulin Isotypes with Profoundly Decreased or Absent B Cells OBS815
Obsolete: Disease with Severe Reduction in Serum Iga and Igg with Normal/elevated Igm and Normal Numbers of B Cells OBS816
Obsolete: Disorder in the Hormonal Synthesis with or Without Goiter OBS513
Obsolete: Disorder with Acute Infantile Liver Failure OBS486
Obsolete: Distal Spinal Muscular Atrophy OBS233
Obsolete: Drug and/or Toxic Myopathy OBS246
Obsolete: Duplication 4q OBS116
Obsolete: Dwarfism-Intellectual Disability-Eye Abnormality Syndrome OBS191
Obsolete: Dysharmonic Micromelia OBS625
Obsolete: Dysmorphic Syndrome Associated with Bone Anomaly OBS624
Obsolete: Early Infantile Epileptic Encephalopathy Without Suppression Burst OBS374
Obsolete: Ectodermal Dysplasia-Absent Dermatoglyphs Syndrome OBS128
Obsolete: Ectodermal Malformation Syndrome Associated with Ocular Features OBS750
Obsolete: Ehlers-Danlos Syndrome Type 1 OBS551
Obsolete: Ehlers-Danlos Syndrome Type 2 OBS550
Obsolete: Ehlers-Danlos Syndrome Type 7a OBS841
Obsolete: Ehlers-Danlos Syndrome Type 7b OBS842
Obsolete: Ehlers-Danlos Syndrome, Fibronectinemic Type OBS532
Obsolete: Embryonary Disorganization Syndrome OBS251
Obsolete: Endocrine Myopathy OBS245
Obsolete: Epicanthal Fold OBS702
Obsolete: Epidermal Nevus-Vitamin D-Resistant Rickets Syndrome OBS175
Obsolete: Epimetaphyseal Skeletal Dysplasia OBS095
Obsolete: Epithelio-Exfoliative Colitis-Deafness Syndrome OBS812
Obsolete: Erythromelalgia OBS154
Obsolete: Eyebrow Hypertrophy OBS684
Obsolete: Eyebrow/eyelashes Distichiasis OBS678
Obsolete: Eyebrow/eyelashes Hypertrichosis OBS685
Obsolete: Eyebrow/eyelashes Pigmentation Anomaly OBS676
Obsolete: Eyebrow/eyelashes Structural Anomaly OBS677
Obsolete: Eyelashes Hypertrophy OBS683
Obsolete: Facial Asymmetry-Temporal Seizures Syndrome OBS254
Obsolete: Familial Articular Chondrocalcinosis Type 1 OBS847 CCAL1
Obsolete: Familial Articular Chondrocalcinosis Type 2 OBS848 CCAL2
Obsolete: Familial Capillary Hemangioma OBS558
Obsolete: Familial Esophageal Achalasia OBS662
Obsolete: Familial Flecked Retinopathy OBS268
Obsolete: Familial Intestinal Malrotation-Facial Anomalies Syndrome OBS165
Obsolete: Familial Pseudohyperkalemia Type 2 OBS833
Obsolete: Familial Pseudohyperkalemia, Cardiff Type OBS834
Obsolete: Familial Renal Cell Carcinoma OBS109
Obsolete: Familial Restrictive Cardiomyopathy Type 1 OBS837
Obsolete: Familial Restrictive Cardiomyopathy Type 2 OBS836
Obsolete: Familial Restrictive Cardiomyopathy Type 3 OBS266 RCM3
Obsolete: Familial Segmental Neurofibromatosis OBS561
Obsolete: Familial Spinal Neurofibromatosis OBS562
Obsolete: Fatal Infantile Hypertrophic Cardiomyopathy Due to Mitochondrial Complex I Deficiency OBS421
Obsolete: Femoral Agenesis/hypoplasia, Bilateral OBS402
Obsolete: Femoral Agenesis/hypoplasia, Unilateral OBS403
Obsolete: Fibrocalculous Pancreatopathy OBS653 FCPD
Obsolete: Fibular Aplasia-Tibial Campomelia-Oligosyndactyly Syndrome OBS516
Obsolete: Fibular Hemimelia, Bilateral OBS394
Obsolete: Fibular Hemimelia, Unilateral OBS395
Obsolete: Fluindione Toxicity OBS284
Obsolete: Follicular Hamartoma-Alopecia-Cystic Fibrosis Syndrome OBS158
Obsolete: Fosphenytoin Toxicity OBS297
Obsolete: Gastric Neuroendocrine Tumor Type 1 OBS519
Obsolete: Gastric Neuroendocrine Tumor Type 2 OBS517
Obsolete: Gastric Neuroendocrine Tumor Type 3 OBS518
Obsolete: Gastric Neuroendocrine Tumor Type 4 OBS520
Obsolete: Generalized Epilepsy and Praxis-Induced Seizures OBS659
Obsolete: Genetic Cerebrovascular Dementia OBS490
Obsolete: Genetic Keratinization Disorder Associated with Ocular Features OBS741
Obsolete: Genetic Macular Dystrophy OBS714
Obsolete: Genetic Muscular Channelopathy OBS381
Obsolete: Genetic Neurological Channelopathy OBS732
Obsolete: Genetic Optic Atrophy OBS488
Obsolete: Genetic Vitreous-Retinal Disease OBS716
Obsolete: Genodermatosis with Ocular Features OBS738
Obsolete: Giant Infantile Hemangioma OBS259
Obsolete: Glaucoma Associated with Neural Crest Cell Migration Anomaly OBS722
Obsolete: Glibenclamide Toxicity OBS286
Obsolete: Gliclazide Toxicity OBS285
Obsolete: Glimepiride Toxicity OBS288
Obsolete: Glipizide Toxicity OBS287
Obsolete: Glycogen Storage Disease Due to Acid Maltase Deficiency, Adult Onset OBS425
Obsolete: Glycogen Storage Disease Due to Acid Maltase Deficiency, Juvenile Onset OBS426
Obsolete: Gmppb-Related Congenital Muscular Dystrophy OBS377
Obsolete: Goniodysgenesis OBS723
Obsolete: Graft Rejection After Lung Transplantation OBS559
Obsolete: Granulomatous Myositis OBS234
Obsolete: Grix-Blankenship-Peterson Syndrome OBS160
Obsolete: Harmonic Micromelia OBS628
Obsolete: Heckenlively Syndrome OBS159
Obsolete: Heinz Body Anemia OBS097
Obsolete: Hemihypertrophy-Intestinal Web-Corneal Opacity Syndrome OBS157
Obsolete: Hemolytic Anemia Due to Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency OBS163
Obsolete: Hepatic Amyloidosis with Intrahepatic Cholestasis OBS819
Obsolete: Hereditary Acrokeratotic Poikiloderma of Kindler-Weary OBS428
Obsolete: Hereditary Epidermolysis Bullosa Associated with Ocular Features OBS198
Obsolete: Hereditary Iron Overload with Anemia OBS148
Obsolete: Hereditary Iron Overload with Neurologic Manifestation OBS149
Obsolete: Hereditary Resistance to Anti-Vitamin K OBS509
Obsolete: Hereditary Thrombocytopenia-Hematological Cancer Predisposition Syndrome OBS522
Obsolete: Heredodegenerative Disease with Dystonia As a Major Feature OBS601
Obsolete: Hiv-Related Anal Cancer OBS500
Obsolete: Hiv-Related Cervical Cancer OBS505
Obsolete: Hiv-Related Hepatocellular Carcinoma OBS501
Obsolete: Hiv-Related Hodgkin Lymphoma OBS503
Obsolete: Hiv-Related Kaposi Sarcoma OBS497
Obsolete: Hiv-Related Lung Cancer OBS498
Obsolete: Hiv-Related Non-Hodgkin Lymphoma OBS496
Obsolete: Hiv-Related Oropharyngeal Cancer OBS499
Obsolete: Hiv-Related Penile Cancer OBS502
Obsolete: Hiv-Related Vulvovaginal Cancer OBS504
Obsolete: Holoacardius Amorphus OBS253
Obsolete: Humeral Agenesis/hypoplasia, Bilateral OBS400
Obsolete: Humeral Agenesis/hypoplasia, Unilateral OBS401
Obsolete: Humero-Radial Synostosis, Bilateral OBS480
Obsolete: Humero-Radial Synostosis, Unilateral OBS479
Obsolete: Humero-Radio-Ulnar Synostosis, Bilateral OBS482
Obsolete: Humero-Radio-Ulnar Synostosis, Unilateral OBS481
Obsolete: Hyperlipoproteinemia Type 5 OBS084
Obsolete: Hyperphalangy, Bilateral OBS458
Obsolete: Hyperphalangy, Unilateral OBS457
Obsolete: Hypertrichotic Osteochondrodysplasia OBS183
Obsolete: Hypodermyiasis OBS512
Obsolete: Hypopituitarism-Postaxial Polydactyly Syndrome OBS170
Obsolete: Hypopituitarism-Short Stature-Skeletal Anomalies Syndrome OBS240
Obsolete: Ichthyosis Associated with a Cornified Cell Envelope and Epidermal Lipid Metabolism Anomaly OBS780
Obsolete: Ichthyosis Associated with a Nucleotide Excision Repair Anomaly OBS781
Obsolete: Ichthyosis Associated with a Peroxisomal Disease OBS778
Obsolete: Ichthyosis Associated with a Protein Catabolism Anomaly OBS779
Obsolete: Ichthyosis Associated with Ocular Features OBS740
Obsolete: Ichthyosis-Cheek-Eyebrow Syndrome OBS169
Obsolete: Idiopathic Hydrops Fetalis OBS547
Obsolete: Idiopathic Hypersomnia with Long Sleep Time OBS272
Obsolete: Idiopathic Hypersomnia Without Long Sleep Time OBS271
Obsolete: Imipramine Toxicity OBS278
Obsolete: Immunoglobulin A1 Deficiency OBS840
Obsolete: Immunoglobulin A2 Deficiency OBS839
Obsolete: Immunoproliferative Small Intestinal Disease OBS810 IPSID
Obsolete: Indian Tick Typhus OBS825
Obsolete: Infantile Axonal Neuropathy OBS174
Obsolete: Infantile Non-Syndromic Cataract OBS263
Obsolete: Infantile Striatothalamic Degeneration OBS143
Obsolete: Infantile Symmetrical Thalamic Degeneration OBS220
Obsolete: Infantile Thalamic Degeneration OBS144
Obsolete: Inflammatory/autoimmune Optic Neuropathy OBS545
Obsolete: Inherited Predisposition to Essential Thrombocythemia OBS269
Obsolete: Intellectual Disability-Hypotonia-Skin Hyperpigmentation Syndrome OBS195
Obsolete: Intellectual Disability-Microcephaly-Phalangeal-Facial Abnormalities Syndrome OBS202
Obsolete: Intellectual Disability-Microcephaly-Unusual Facies Syndrome OBS212
Obsolete: Intellectual Disability-Unusual Facies Syndrome OBS197
Obsolete: Intellectual Disability-Unusual Facies, Davis-Lafer Type OBS196
Obsolete: Intermediate Stomatocytosis Syndrome OBS651
Obsolete: Intracranial Aneurysms-Multiple Congenital Anomalies Syndrome OBS118
Obsolete: Intramural Coronary Arterial Course OBS643
Obsolete: Joker Disease OBS161
Obsolete: Juvenile Chronic Recurrent Multifocal Osteomyelitis OBS264
Obsolete: Juvenile Parkinsonism with Intellectual Disability Due to Dnajc6 Deficiency OBS383
Obsolete: Juvenile-Onset Sapho Syndrome OBS372
Obsolete: Kenya Tick Typhus OBS824
Obsolete: Keratoconus OBS141
Obsolete: Kinetic Eyelid Anomaly OBS694
Obsolete: Laminopathy Type Decaudain-Vigouroux OBS129
Obsolete: Laryngeal Dyskinesia OBS635
Obsolete: Laryngo-Tracheo-Esophageal Cleft-Pulmonary Hypoplasia Syndrome OBS096
Obsolete: Late-Onset Primary Lymphedema OBS419
Obsolete: Lethal Brachymelia-Polycystic Kidney Disease-Congenital Heart Defect Syndrome OBS489
Obsolete: Lethal Chondrodysplasia, Moerman Type OBS138
Obsolete: Lethal Chondrodysplasia, Seller Type OBS139
Obsolete: Lethal Idiopathic Viral Infection OBS539
Obsolete: Levodopa-Unresponsive Juvenile Parkinsonism OBS384
Obsolete: Limb Dystonia OBS637
Obsolete: Limb-Girdle Bone Anomaly OBS627
Obsolete: Limbic Encephalitis with Ncmags Antibodies OBS086
Obsolete: Lissencephaly-Demyelinating Axonal Neuropathy Syndrome OBS822
Obsolete: Localized Epiphyseal Dysplasia OBS155
Obsolete: Low Birth Weight-Dwarfism-Dysgammaglobulinemia Syndrome OBS188
Obsolete: Low-Grade Ependymoma OBS167
Obsolete: Lymphedema Praecox OBS534
Obsolete: Lymphedema Tarda OBS533
Obsolete: Lymphedema-Cleft Palate Syndrome OBS553
Obsolete: Lymphocytic Colitis OBS526
Obsolete: Macrocephaly-Immune Deficiency-Anemia Syndrome OBS638
Obsolete: Maculopapular Lupus Rash OBS552
Obsolete: Major Induction Processes Eye Anomaly OBS704
Obsolete: Male Infertility with Impaired Virilization OBS777
Obsolete: Male Infertility with Impaired Virilization Due to a Hypothalamic and Pituitary Disorder Associated with Hyperprolactinemia OBS791
Obsolete: Male Infertility with Impaired Virilization Due to a Testicular Disorder OBS792
Obsolete: Male Infertility with Impaired Virilization Due to a Testicular Disorder Associated with a Chronic Illness OBS789
Obsolete: Male Infertility with Impaired Virilization Due to a Testicular Disorder Associated with a Hepatic Disease OBS788
Obsolete: Male Infertility with Impaired Virilization Due to a Testicular Disorder Associated with a Neurologic Disease OBS769
Obsolete: Male Infertility with Impaired Virilization Due to a Testicular Disorder Associated with a Systemic Disease OBS782
Obsolete: Male Infertility with Impaired Virilization Due to a Testicular Disorder Associated with an Immune Disorder OBS787
Obsolete: Male Infertility with Impaired Virilization Due to a Testicular Disorder Associated with Renal Failure OBS783
Obsolete: Male Infertility with Impaired Virilization Due to a Testicular Disorder Associated with Thyrotoxicosis OBS786
Obsolete: Male Infertility with Impaired Virilization Due to a Viral Orchitis OBS795
Obsolete: Male Infertility with Impaired Virilization Due to an Acquired Testicular Defect OBS790
Obsolete: Male Infertility with Impaired Virilization Due to an Acquired Testicular Defect Associated with a Granulomatous Disease OBS785
Obsolete: Male Infertility with Impaired Virilization Due to an Acquired Testicular Defect Associated with an Environmental Toxin OBS794
Obsolete: Male Infertility with Impaired Virilization Due to an Acquired Testicular Defect Associated with Autoimmunity OBS784
Obsolete: Male Infertility with Impaired Virilization Due to an Acquired Testicular Defect Associated with Trauma OBS796
Obsolete: Male Infertility with Impaired Virilization Due to an Acquired Testicular Defect Drug-Related OBS793
Obsolete: Male Infertility with Impaired Virilization Due to an Hypothalamic or Pituitary Disorder OBS776
Obsolete: Male Infertility with Normal Virilization OBS768
Obsolete: Male Infertility with Normal Virilization Due to a Developmental or Structural Testicular Defect OBS772
Obsolete: Male Infertility with Normal Virilization Due to a Developmental or Structural Testicular Defect Associated with Cryptorchidism OBS775
Obsolete: Male Infertility with Normal Virilization Due to a Developmental or Structural Testicular Defect Associated with Varicocele OBS774
Obsolete: Male Infertility with Normal Virilization Due to a Hypothalamic or Pituitary Defect OBS771
Obsolete: Male Infertility with Normal Virilization Due to a Systemic Disease OBS767
Obsolete: Male Infertility with Normal Virilization Due to a Testicular Defect OBS773
Obsolete: Male Infertility with Normal Virilization Due to Acquired Testicular Defect Associated with Autoimmunity OBS764
Obsolete: Male Infertility with Normal Virilization Due to an Acquired Testicular Defect OBS761
Obsolete: Male Infertility with Normal Virilization Due to an Acquired Testicular Defect Associated with Drug OBS762
Obsolete: Male Infertility with Normal Virilization Due to an Acquired Testicular Defect Associated with Environmental Toxin OBS765
Obsolete: Male Infertility with Normal Virilization Due to an Acquired Testicular Defect Associated with Mycoplasma Infection OBS760
Obsolete: Male Infertility with Normal Virilization Due to an Acquired Testicular Defect Associated with Radiation OBS763
Obsolete: Male Infertility with Normal Virilization Due to Androgen Administration OBS770
Obsolete: Male Infertility with Normal Virilization Due to Testicular Defect Associated with Spinal Cord Injury OBS766
Obsolete: Malignant Tumor of Palpebral Epidermis OBS688
Obsolete: Mandibulofacial Dysostosis-Deafness-Postaxial Polydactyly Syndrome OBS257
Obsolete: Mandibulofacial Dysostosis-Lymphedema Syndrome OBS649
Obsolete: Marseilles Fever OBS821
Obsolete: Maternally-Inherited Mitochondrial Hypertrophic Cardiomyopathy OBS180
Obsolete: Mclain-Dekaban Syndrome OBS166
Obsolete: Mediterranean Spotted Fever OBS820
Obsolete: Melanoma-Pancreatic Cancer Syndrome OBS540
Obsolete: Mercaptopurine Dose Selection in the Treatment of Crohn Disease, Leukemia and in Transplantation OBS294
Obsolete: Mercaptopurine Toxicity OBS279
Obsolete: Mesenchymatous Palpebral Tumor OBS681
Obsolete: Metabolic Disease Associated with Ocular Features OBS749
Obsolete: Metabolic Disease with Cataract OBS736
Obsolete: Metabolic Disease with Corneal Opacity OBS735
Obsolete: Metabolic Disease with Macular Cherry-Red Spot OBS734
Obsolete: Metabolic Disease with Pigmentary Retinitis OBS733
Obsolete: Metastatic Pituitary Hormone Deficiency OBS614
Obsolete: Metastatic Spermatocytic Seminoma OBS844
Obsolete: Metatropic Dysplasias OBS629
Obsolete: Methotrexate Dose Selection OBS429
Obsolete: Methotrexate Poisoning OBS544
Obsolete: Mickleson Syndrome OBS185
Obsolete: Microcephaly-Seizures-Developmental Delay Syndrome OBS270 MCSZ
Obsolete: Microcornea-Corectopia-Macular Hypoplasia Syndrome OBS186
Obsolete: Microlissencephaly Type B OBS826
Obsolete: Micromelic Dwarfism, Fryns Type OBS189
Obsolete: Microphthalmia-Cataract Syndrome OBS187
Obsolete: Microscopic Colitis OBS528
Obsolete: Miscellaneous Metabolic Disease Associated with Bone Anomaly OBS626
Obsolete: Mitochondrial Disease with Eye Involvement OBS739
Obsolete: Mitochondrial Disorder Due to a Transcription or a Translation Defect of Mitochondrial Dna OBS427
Obsolete: Mivacurium Toxicity OBS281
Obsolete: Mixed Dystonia OBS535
Obsolete: Moderate Spondylodysplastic Dysplasia OBS630
Obsolete: Multifocal Muscular Fibrosis-Obstructed Vessels Syndrome OBS256
Obsolete: Multiple Epiphyseal Dysplasia, Unclassified Type OBS556
Obsolete: Multiple Ventricular Septal Defects OBS648
Obsolete: Myasthenic Syndrome with Eye Involvement OBS752
Obsolete: Myopathy with Eye Involvement OBS751
Obsolete: Natal Teeth-Intestinal Pseudoobstruction-Patent Ductus Syndrome OBS146
Obsolete: Neonatal Membranous Glomerulopathy with Maternal Nep Deficiency OBS605
Obsolete: Nervous System Anomaly with Eye Involvement OBS754
Obsolete: Neuroaxonal Dystrophy-Renal Tubular Acidosis Syndrome OBS173
Obsolete: Neuroendocrine Tumor of Small Intestine OBS511
Obsolete: Neurofibromatosis OBS542
Obsolete: Neurological Channelopathy OBS152
Obsolete: Neurosensory Deafness-Pituitary Dwarfism Syndrome OBS222
Obsolete: Non-Chondrodysplastic Malformation Syndrome Affecting Bones OBS121
Obsolete: Non-Distal Monosomy 7p OBS616
Obsolete: Non-Dystrophic Myopathy with Collagen 6 Anomaly OBS232
Obsolete: Non-Idiopathic Juvenile Arthritis OBS642
Obsolete: Non-Pore-Loop Channelopathy OBS583
Obsolete: Non-Pore-Loop Channelopathy Due to Cl- Channel Barttin Anomaly OBS571
Obsolete: Non-Pore-Loop Channelopathy Due to Cl- Channel Clc2 Anomaly OBS592
Obsolete: Non-Pore-Loop Channelopathy Due to Cl- Channel Skeletal Muscle Clc1 Anomaly OBS589
Obsolete: Non-Pore-Loop Channelopathy Due to Cl- Channels Kidney Clcka and Clckb Anomaly OBS570
Obsolete: Non-Pore-Loop Channelopathy Due to Cl- Transporter Clc7anomaly OBS569
Obsolete: Non-Pore-Loop Channelopathy Due to Cl- Transporter Kidney Clc5 Anomaly OBS591
Obsolete: Non-Pore-Loop Channelopathy Due to Epithelial Cl- Channel Bestrophin Anomaly OBS590
Obsolete: Non-Pore-Loop Channelopathy Due to Epithelial Cl- Channel Cftr Anomaly OBS587
Obsolete: Non-Pore-Loop Channelopathy Involved in Other Renal Tubular Disorder OBS652
Obsolete: Non-Pore-Loop Channelopathy Involved in Several Types of Epilepsy OBS660
Obsolete: Non-Progressive Congenital Heart Block OBS658
Obsolete: Non-Syndromic Developmental Defect of the Eye OBS814
Obsolete: Nortriptyline Toxicity OBS280
Obsolete: Not Notch3-Related Small Vessel Disease of the Brain OBS531
Obsolete: Nuclear Cell Envelopathy OBS818
Obsolete: Nuclear Oculomotor Paralysis OBS831
Obsolete: Ocular Coloboma OBS111
Obsolete: Oculocerebroacral Syndrome OBS179
Obsolete: Oculocerebroosseous Syndrome OBS181
Obsolete: Oculo-Skeletal-Renal Syndrome OBS177
Obsolete: Onycho-Patellar Syndrome with Eye Involvement OBS746
Obsolete: Ophthalmoplegia-Myalgia-Tubular Aggregates Syndrome OBS182
Obsolete: Other Forms of Non-Paraneoplastic Limbic Encephalitis OBS085
Obsolete: Other Ganglionopathy Related to Autoimmune Diseases OBS248
Obsolete: Other Muscle Weakness and/or Chronic Muscle Pain OBS236
Obsolete: Otopalatodigital Syndrome OBS231
Obsolete: Palpebral Epidermal Tumor OBS697
Obsolete: Palpebral Lentiginosis OBS693
Obsolete: Palpebral Malignant Melanoma OBS691
Obsolete: Palpebral Nevus OBS692
Obsolete: Palpebral Piliary Tumor OBS690
Obsolete: Palpebral Sebaceous Gland Tumor OBS687
Obsolete: Palpebral Tumor OBS696
Obsolete: Palpebral Tumor with a Vascular Malformation OBS680
Obsolete: Pancreatic Beta Cell Agenesis with Neonatal Diabetes Mellitus OBS508
Obsolete: Pancuronium Toxicity OBS283
Obsolete: Papillary Fibroelastoma of the Heart OBS249
Obsolete: Paraplegia-Brachydactyly-Cone-Shaped Epiphysis Syndrome OBS184
Obsolete: Partial Prune Belly Syndrome OBS555
Obsolete: Patella Aplasia/hypoplasia, Bilateral OBS407
Obsolete: Patella Aplasia/hypoplasia, Unilateral OBS406
Obsolete: Pediatric Polyarteritis Nodosa OBS618
Obsolete: Pediatric Sjogren Syndrome OBS619
Obsolete: Pediatric Systemic Sclerosis OBS620
Obsolete: Peters Anomaly-Cataract Syndrome OBS828
Obsolete: Phakomatosis with Eye Involvement OBS745
Obsolete: Phenprocoumon Toxicity OBS282
Obsolete: Phenytoin Toxicity OBS296
Obsolete: Phosphoenolpyruvate Carboxykinase 1 Deficiency OBS563
Obsolete: Phosphoenolpyruvate Carboxykinase 2 Deficiency OBS564
Obsolete: Pierre Robin Syndrome Associated with Miscellaneous Anomalies OBS135
Obsolete: Pigmentation Disorder with Eye Involvement OBS742
Obsolete: Pigmentation Disorder with Eye Involvement, Excluding Albinism OBS748
Obsolete: Pigmented Conjunctival Lesion OBS727
Obsolete: Pigmented Palpebral Tumor OBS686
Obsolete: Pili Canulati OBS515
Obsolete: Pilotto Syndrome OBS203
Obsolete: Pituitary Deficiency Secondary to an Anevrysm OBS610
Obsolete: Pituitary Deficiency Secondary to Meningeal Hemorrhage OBS611
Obsolete: Platelet Function Disease Associated with Renal Insufficiency OBS650
Obsolete: Platelet Storage Pool Disease OBS801 SPD
Obsolete: Platyspondylic Lethal Chondrodysplasia OBS093
Obsolete: Pleomorphic Undifferentiated Sarcoma OBS420
Obsolete: Polydactyly of a Biphalangeal Thumb, Bilateral OBS460
Obsolete: Polydactyly of a Biphalangeal Thumb, Unilateral OBS459
Obsolete: Polydactyly of a Triphalangeal Thumb, Bilateral OBS462
Obsolete: Polydactyly of a Triphalangeal Thumb, Unilateral OBS461
Obsolete: Polydactyly of an Index Finger, Bilateral OBS467
Obsolete: Polydactyly of an Index Finger, Unilateral OBS463
Obsolete: Polymicrogyria-Turricephaly-Hypogenitalism Syndrome OBS209
Obsolete: Polysyndactyly, Bilateral OBS465
Obsolete: Polysyndactyly, Unilateral OBS466
Obsolete: Pore-Loop Channelopathy OBS596
Obsolete: Postaxial Polydactyly of Fingers OBS385
Obsolete: Postaxial Polydactyly of Toes OBS411
Obsolete: Postaxial Polydactyly of Toes, Bilateral OBS478
Obsolete: Postaxial Polydactyly of Toes, Unilateral OBS472
Obsolete: Postaxial Polydactyly Type a, Bilateral OBS471
Obsolete: Postaxial Polydactyly Type a, Unilateral OBS464
Obsolete: Postaxial Polydactyly Type B, Bilateral OBS469
Obsolete: Postaxial Polydactyly Type B, Unilateral OBS470
Obsolete: Posterior Fossa Tumors OBS657
Obsolete: Postsurgical Hypopituitarism OBS609
Obsolete: Posttraumatic Diabetes Insipidus OBS612
Obsolete: Posttraumatic Hypopituitarism OBS613
Obsolete: Posttraumatic Syringomyelia OBS845
Obsolete: Pravastatin Toxicity OBS298
Obsolete: Preaxial Polydactyly of Toes OBS412
Obsolete: Preaxial Polydactyly of Toes, Bilateral OBS473
Obsolete: Preaxial Polydactyly of Toes, Unilateral OBS474
Obsolete: Precancerous Lesion of Palpebral Epidermis OBS689
Obsolete: Preeyasombat-Varavithya Syndrome OBS208
Obsolete: Primary Syringomyelia/hydromyelia OBS204
Obsolete: Primary T Cell Immunodeficiency OBS274
Obsolete: Progeria-Associated Arthropathy OBS663
Obsolete: Progressive Epilepsy and/or Ataxia with Myoclonus As a Major Feature OBS423
Obsolete: Protease Inhibitor Anomaly OBS800
Obsolete: Pulmonary Aortic Stenosis Obstructive Uropathy OBS131
Obsolete: Pulmonary Artery/pulmonary Branch Anomaly OBS737
Obsolete: Pulmonary Vein Atresia OBS646
Obsolete: Radial Hemimelia, Bilateral OBS404
Obsolete: Radial Hemimelia, Unilateral OBS405
Obsolete: Radiation-Induced Hypopituitarism OBS608
Obsolete: Ramsay Hunt Syndrome Type Ii OBS506
Obsolete: Rare Acquired Eye Disease OBS823
Obsolete: Rare Bone Disease with Limb Reduction Defect OBS370
Obsolete: Rare Disease in Physical Medicine and Rehabilitation OBS595
Obsolete: Rare Disease with Corpus Callosum Agenesis Associated with Peripheral Neuropathy OBS241
Obsolete: Rare Eye Disease Due to a Differentiation Anomaly OBS705
Obsolete: Rare Genetic Deafness OBS603
Obsolete: Rare Genetic Glaucoma OBS107
Obsolete: Rare Genetic Palpebral, Lacrimal System and Conjunctival Disease OBS108
Obsolete: Rare Genetic Refraction Anomaly OBS106
Obsolete: Rare Glaucoma OBS724
Obsolete: Rare Hereditary Iron Overload Disease OBS376
Obsolete: Rare Inflammatory Eye Disease OBS110
Obsolete: Rare Major Hypertriglyceridemia OBS112
Obsolete: Rare Non-Syndromic Cataract OBS261
Obsolete: Rare Palpebral, Lacrimal System and Conjunctival Disease OBS703
Obsolete: Recessive Aplasia Cutis Congenita of Limbs OBS119
Obsolete: Recessive Hereditary Methemoglobinemia Type 1 OBS124
Obsolete: Recessive Hereditary Methemoglobinemia Type 2 OBS125
Obsolete: Rejection After Corneal Transplantation OBS546
Obsolete: Renal Cell Carcinoma Associated with Neuroblastoma OBS373
Obsolete: Resistance to Acenocoumarol in Venous Thrombosis and Atrial Fibrillation OBS295
Obsolete: Resistance to Amitriptyline in the Treatment of Depression OBS352
Obsolete: Resistance to Clomipramine in the Treatment of Depression OBS351
Obsolete: Resistance to Fluindione in Venous Thrombosis and Atrial Fibrillation OBS350
Obsolete: Resistance to Imipramine in the Treatment of Depression OBS349
Obsolete: Resistance to Nortripilline in the Treatment of Depression OBS348
Obsolete: Resistance to Phenprocoumon in Venous Thrombosis and Atrial Fibrillation OBS347
Obsolete: Resistance to Tacrolimus in Transplantation OBS346
Obsolete: Resistance to Trimipramine in the Treatment of Depression OBS345
Obsolete: Resistance to Venlafaxine in the Treatment of Depression OBS344
Obsolete: Resistance to Warfarine in Venous Thrombosis and Atrial Fibrillation OBS343
Obsolete: Retinitis Pigmentosa and Intellectual Disability Due to Monosomy Xp11.3 OBS190
Obsolete: Retrocerebellar Cyst OBS216
Obsolete: Rocuronium Toxicity OBS299
Obsolete: Rosselli-Gulienetti Syndrome OBS548
Obsolete: Rosuvastatin Toxicity OBS300
Obsolete: Sakati-Nyhan Syndrome OBS199
Obsolete: Satracurium Toxicity OBS301
Obsolete: Secondary Ciliary Dyskinesia OBS557 SCD
Obsolete: Secondary Entropion OBS700
Obsolete: Secondary Glaucoma Due to a Proliferation and Differentiation Anomaly OBS721
Obsolete: Secretory Apparatus of the Lacrimal System Anomaly OBS679
Obsolete: Sequence or Association OBS122
Obsolete: Short Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency OBS536
Obsolete: Short Stature-Heart Defect-Craniofacial Anomalies Syndrome OBS117
Obsolete: Short Stature-Microcephaly-Heart Defect Syndrome OBS207
Obsolete: Short Stature-Prognathism-Short Femoral Necks Syndrome OBS206
Obsolete: Shy-Drager Syndrome OBS665 SDS
Obsolete: Simvastatin Toxicity OBS302
Obsolete: Single Ventricular Septal Defect OBS647
Obsolete: Sinus Node Disease-Myopia Syndrome OBS200
Obsolete: Slc5a6-Cdg OBS554
Obsolete: Small Pox OBS507
Obsolete: Solitary Median Maxillary Central Incisor Syndrome OBS172 SMMCI
Obsolete: Spherocytic Elliptocytosis OBS664
Obsolete: Spinocerebellar Ataxia with Oculomotor Anomaly OBS755
Obsolete: Spinocerebellar Degenerescence and Spastic Paraparesis with an Oculomotor Anomaly OBS756
Obsolete: Split Foot OBS414
Obsolete: Split Foot, Bilateral OBS450
Obsolete: Split Foot, Unilateral OBS449
Obsolete: Split Hand OBS415
Obsolete: Split Hand or/and Split Foot Malformation OBS388
Obsolete: Split Hand, Bilateral OBS448
Obsolete: Split Hand, Unilateral OBS446
Obsolete: Spondyloepimetaphyseal Dysplasia OBS218
Obsolete: Sporadic Achalasia OBS661
Obsolete: Sporadic Leigh Syndrome OBS178
Obsolete: Squamous Cell Carcinoma of Head and Neck OBS525 HNSCC
Obsolete: Subcutaneous Myiasis OBS088
Obsolete: Susceptibility to Adverse Reaction Due to 5-Fluorouracil Treatment OBS342
Obsolete: Susceptibility to Adverse Reaction Due to Amitriptyline Treatment OBS341
Obsolete: Susceptibility to Adverse Reaction Due to Antipsychotics Treatment OBS340
Obsolete: Susceptibility to Adverse Reaction Due to Atorvastatin Treatment OBS339
Obsolete: Susceptibility to Adverse Reaction Due to Capecitabine Treatment OBS367
Obsolete: Susceptibility to Adverse Reaction Due to Clomipramine Treatment OBS368
Obsolete: Susceptibility to Adverse Reaction Due to Codeine Treatment OBS365
Obsolete: Susceptibility to Adverse Reaction Due to Efavirenz Treatment OBS366
Obsolete: Susceptibility to Adverse Reaction Due to Imipramine Treatment OBS363
Obsolete: Susceptibility to Adverse Reaction Due to Irinotecan Treatment OBS364
Obsolete: Susceptibility to Adverse Reaction Due to Isoniazide Treatment OBS361
Obsolete: Susceptibility to Adverse Reaction Due to Methotrexate Treatment OBS362
Obsolete: Susceptibility to Adverse Reaction Due to Nortriptyline Treatment OBS359
Obsolete: Susceptibility to Adverse Reaction Due to Pravastatin Treatment OBS360
Obsolete: Susceptibility to Adverse Reaction Due to Rosuvastatin Treatment OBS357
Obsolete: Susceptibility to Adverse Reaction Due to Simvastatin Treatment OBS358
Obsolete: Susceptibility to Adverse Reaction Due to Trimipramine Treatment OBS355
Obsolete: Susceptibility to Adverse Reaction Due to Venlafaxine Treatment OBS356
Obsolete: Susceptibility to Bleeding Due to Acenocoumarol Treatment OBS353
Obsolete: Susceptibility to Bleeding Due to Fluindione Treatment OBS354
Obsolete: Susceptibility to Bleeding Due to Phenprocoumon Treatment OBS327
Obsolete: Susceptibility to Bleeding Due to Warfarine Treatment OBS326
Obsolete: Susceptibility to Deafness Due to Cisplatin Treatment OBS329
Obsolete: Susceptibility to Hepatitis Due to Flucloxacilline Treatment OBS328
Obsolete: Susceptibility to Hepatitis Due to Voriconazole Treatment OBS323
Obsolete: Susceptibility to Hypersensitivity Syndrome Due to Abacavir Treatment OBS322
Obsolete: Susceptibility to Hypoglycemia Due to Carbutamide Treatment OBS325
Obsolete: Susceptibility to Hypoglycemia Due to Glibenclamide Treatment OBS324
Obsolete: Susceptibility to Hypoglycemia Due to Gliclazide Treatment OBS319
Obsolete: Susceptibility to Hypoglycemia Due to Glimepiride Treatment OBS318
Obsolete: Susceptibility to Hypoglycemia Due to Glipizide Treatment OBS321
Obsolete: Susceptibility to Icterus Due to Raltegravir Treatment OBS320
Obsolete: Susceptibility to Myopathies Due to Statin Treatment OBS430
Obsolete: Susceptibility to Neutropenia Due to Azathioprine Treatment OBS315
Obsolete: Susceptibility to Neutropenia Due to Mercaptopurine Treatment OBS314
Obsolete: Susceptibility to Prolonged Paralysis Due to Cisatracurium Treatment OBS317
Obsolete: Susceptibility to Prolonged Paralysis Due to Mivacurium Treatment OBS316
Obsolete: Susceptibility to Prolonged Paralysis Due to Pancuronium Treatment OBS335
Obsolete: Susceptibility to Prolonged Paralysis Due to Rocuronium Treatment OBS336
Obsolete: Susceptibility to Prolonged Paralysis Due to Satracurium Treatment OBS337
Obsolete: Susceptibility to Prolonged Paralysis Due to Vecuronium Treatment OBS338
Obsolete: Susceptibility to Toxic Epidermal Necrolysis Due to Allopurinol Treatment OBS331
Obsolete: Susceptibility to Toxic Epidermal Necrolysis Due to Carbamazepine Treatment OBS332
Obsolete: Susceptibility to Toxic Epidermal Necrolysis Due to Phenytoin Treatment OBS333
Obsolete: Susceptibility to Toxic Epidermal Necrolysis Due to Phosphenytoin Treatment OBS334
Obsolete: Symbrachydactyly of Hand and Foot, Bilateral OBS456
Obsolete: Symbrachydactyly of Hand and Foot, Unilateral OBS455
Obsolete: Syndrome Associated with a Congenital Cardiopathy OBS731
Obsolete: Syndrome Associated with Pierre Robin Syndrome OBS134
Obsolete: Syndromes with Synostoses of Limbs OBS418
Obsolete: Syndromic Developmental Defect of the Eye OBS813
Obsolete: Syndromic Frontonasal Dysplasia OBS491
Obsolete: Syndromic Ichthyosis Associated with Ocular Features OBS743
Obsolete: Syndromic Malformation of the Optic Disc OBS543
Obsolete: Syndromic Myopia OBS725
Obsolete: Systemic Disease with Cataract OBS718
Obsolete: Systemic Non-Langerhans Cell Histiocytosis OBS303
Obsolete: Tachycardia-Hypertension-Microphthalmos-Hyperglycinuria Syndrome OBS219
Obsolete: Taci-Related Selective Deficiency of Iga OBS838
Obsolete: Tauopathy OBS805
Obsolete: Tauopathy with a Major Tau at 60 Kda OBS804
Obsolete: Tauopathy with a Major Tau Doublet at 60 and 64 Kda OBS803
Obsolete: Tauopathy with a Major Tau Doublet at 64 and 69 Kda OBS808
Obsolete: Tauopathy with a Major Tau Triplet at 60, 64 and 69 Kda OBS807
Obsolete: Tauopathy with Non-Alzheimer Non-Pick Frontal Lobe Degeneration OBS806
Obsolete: Taussig-Bing Syndrome OBS827
Obsolete: Terminal Limb Defects OBS389
Obsolete: Terminal Transverse Defects of Arm OBS640
Obsolete: Thyroid Pyramidal Lobe OBS617
Obsolete: Tibial Hemimelia, Bilateral OBS392
Obsolete: Tibial Hemimelia, Unilateral OBS393
Obsolete: Torres-Aybar Syndrome OBS214
Obsolete: Toxic or/and Iatrogenic Neuropathy OBS239
Obsolete: Tracheo-Esophageal Fistula-Hypospadias Syndrome OBS162
Obsolete: Transient Neonatal Arthrogryposis OBS132
Obsolete: Trichodermal Syndrome-Intellectual Disability Syndrome OBS255
Obsolete: Trichomegaly-Cataract-Hereditary Spherocytosis Syndrome OBS210
Obsolete: Tricho-Oculo-Dermo-Vertebral Syndrome OBS213
Obsolete: Trimipramine Toxicity OBS289
Obsolete: Trochlear Nerve Palsy OBS654
Obsolete: True Vascular Thoracic Outlet Syndrome OBS832
Obsolete: Truncal Dystonia OBS636
Obsolete: Type 1 Interferonopathy with Immunodeficiency OBS487
Obsolete: Ulnar Hemimelia, Bilateral OBS391
Obsolete: Ulnar Hemimelia, Unilateral OBS390
Obsolete: Unclassified Autosomal Dominant Spinocerebellar Ataxia OBS597
Obsolete: Unclassified Familial Retinal Dystrophy OBS715
Obsolete: Unclassified Glomerulonephritis OBS606
Obsolete: Unclassified Metaphyseal Chondrodysplasia OBS549
Obsolete: Unclassified Overlapping Connective Tissue Disease OBS171
Obsolete: Unclassified Primitive or Secondary Maculopathy OBS713
Obsolete: Unclassified Spondylometaphyseal Dysplasia OBS091
Obsolete: Unknown Leukodystrophy OBS568
Obsolete: Van Regemorter-Pierquin-Vamos Syndrome OBS215
Obsolete: Vascular Disruption Sequence OBS260
Obsolete: Vascular Malposition OBS514
Obsolete: Vecuronium Toxicity OBS290
Obsolete: Venlafaxine Toxicity OBS291
Obsolete: Vestibular Torticollis OBS655
Obsolete: Vitiligo-Associated Autoimmune Disease OBS164
Obsolete: Vitreoretinal Degeneration OBS710
Obsolete: Von Hippel Anomaly OBS666
Obsolete: Warfarine Dose Selection in the Treatment of Venous Thrombosis and Atrial Fibrillation OBS330
Obsolete: Warfarine Toxicity OBS292
Obsolete: Xeroderma Pigmentosum Complementation Group a OBS224 XPA
Obsolete: Xeroderma Pigmentosum Complementation Group B OBS223 XPB
Obsolete: Xeroderma Pigmentosum Complementation Group C OBS228 XPC
Obsolete: Xeroderma Pigmentosum Complementation Group D OBS227 XPD
Obsolete: Xeroderma Pigmentosum Complementation Group E OBS226 XPE
Obsolete: Xeroderma Pigmentosum Complementation Group F OBS225 XPF
Obsolete: Xeroderma Pigmentosum Complementation Group G OBS229 XPG
Obsolete: X-Linked Dominant Intellectual Disability-Epilepsy Syndrome OBS639
Obsolete: X-Linked Intellectual Disability, Martinez Type OBS194
Obsolete: X-Linked Intellectual Disability, Raynaud Type OBS192
Obsolete: X-Linked Intellectual Disability, Schutz Type OBS193
Obsolete: X-Linked Intellectual Disability, Wittner Type OBS201
Obsolete: X-Linked Intellectual Disability-Obesity-Short Stature Syndrome OBS567
Obsolete: X-Linked Intellectual Disability-Precocious Puberty-Obesity Syndrome OBS566
Obsolete: X-Linked Recessive Hereditary Axonal Motor and Sensory Neuropathy OBS150
Obsolete: X-Linked Recessive Optic Atrophy OBS707
Obsolete: Zlotogura-Martinez Syndrome OBS829
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 Dermatitis OCC001
Ochronosis OCH001
Ocular Albinism OCL001 OA
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 Muscular Dystrophy OCL023
Ocular Myopathy with Curare Sensitivity OCL072
Ocular Neuromyotonia OCL024
Ocular Toxoplasmosis OCL025
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
Oculocerebrodental Syndrome OCL074
Oculocutaneous Albinism OCL002 OCA
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
Oculomotor Apraxia OCL015
Oculomotor Nerve Paralysis OCL003
Oculopalatocerebral Syndrome OCL070
Oculopharyngeal Muscular Dystrophy OCL008 OPMD
Oculopharyngodistal Myopathy OCL063 OPDM
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
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
Oligoarticular Juvenile Idiopathic Arthritis with Anti-Nuclear Antibodies OLG018
Oligoarticular Juvenile Idiopathic Arthritis Without Anti-Nuclear Antibodies OLG019
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
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, Exstrophy of the Cloaca, Imperforate Anus, and Spinal Defects Complex OMP007
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 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
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 Muscular Dystrophy OPH005
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 1 and Deafness OPT022
Optic Atrophy 10 with or Without Ataxia, Mental Retardation, and Seizures OPT062 OPA10
Optic Atrophy 11 OPT064 OPA11
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 Negative Electroretinograms OPT069
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 Hypoplasia, Familial Bilateral OPT030
Optic Nerve Neoplasm OPT008
Optic Nerve Sheath Meningioma OPT002
Optic Neuritis OPT009
Optic Papillitis OPT010
Optic Pathway Glioma OPT032
Opticocochleodentate Degeneration OPT072
Oral and Digital Anomalies with Ichthyosis ORL024
Oral Antidiabetic Drugs Toxicity or Dose Selection ORL023
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 Melanoma ORB015
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
Oropharyngeal Cancer, Adult ORP004
Oropharyngeal Cancer, Childhood ORP005
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
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 Levin Type OST034
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-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 Major Feature OTH014
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 Spectrum Disorders OTP002 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 OTS002 OSMED
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 Tumor with Annular Tubules OVR108
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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