Disease Name Symbol Acronym
Rab18 Deficiency RB1001
Rabies RBS001
Radial Aplasia, X-Linked RDL031
Radial Defect Robin Sequence RDL007
Radial Deficiency-Tibial Hypoplasia Syndrome RDL025
Radial Heads, Posterior Dislocation of RDL035
Radial Hemimelia RDL022
Radial Hypoplasia, Triphalangeal Thumbs and Hypospadias RDL008
Radial Hypoplasia, Triphalangeal Thumbs, Hypospadias, and Maxillary Diastema RDL028
Radial Loop, Plain, on Right Index Finger RDL038
Radial Nerve Lesion RDL001
Radial Neuropathy RDL004
Radial Ray Agenesis RDL009
Radial Ray Deficiency, X-Linked RDL037
Radial Ray Hypoplasia with Choanal Atresia RDL029
Radial-Renal Syndrome RDL030
Radiation Cystitis RDT001
Radiation Induced Angiosarcoma of the Breast RDT003
Radiation Induced Brachial Plexopathy RDT004
Radiation Induced Cancer RDT005
Radiation Myelitis RDT014
Radiation Proctitis RDT013
Radiation Sensitivity of Natural Killer Activity RDT015
Radiation Sensitivity/chromosome Instability Syndrome, Autosomal Dominant RDT007
Radiculoneuropathy, Fatal Neonatal RDC014
Radiculopathy RDC002
Radin Blood Group Antigen RDN004 RD
Radio Renal Syndrome RDR001
Radio-Digito-Facial Dysplasia RDD001
Radio-Ulnar Synostosis Type 1 RDL012
Radio-Ulnar Synostosis Type 2 RDL013
Radio-Ulnar Synostosis-Amegakaryocytic Thrombocytopenia Syndrome RDL039
Radio-Ulnar Synostosis, Bilateral RDL020
Radio-Ulnar Synostosis, Unilateral RDL019
Radiohumeral Fusions with Other Skeletal and Craniofacial Anomalies RDH004
Radioulnar Synostosis RDL002
Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia 1 RDL034
Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia 2 RDL033
Radioulnar Synostosis with Microcephaly, Short Stature, Scoliosis, and Mental Retardation RDL014
Radioulnar Synostosis-Microcephaly-Scoliosis Syndrome RDL026
Radioulnar Synostosis, Radial Ray Abnormalities, and Severe Malformations in the Male RDL036
Radioulnar Synostosis, Unilateral, with Developmental Retardation and Hypotonia RDL032
Radius Absent Anogenital Anomalies RDS001
Radius, Aplasia of, with Cleft Lip/palate RDS005
Ragweed Sensitivity RGW001
Rahman Syndrome RHM034
Rainbow Trout Allergy RNB001
Raindrop Hypopigmentation RND003
Raine Syndrome RNS001
Rajab Syndrome RJB001
Raltegravir Toxicity RLT001
Ramer Ladda Syndrome RMR001
Ramon Syndrome RMN002
Ramos Arroyo Clark Syndrome RMS002
Ramsay Hunt Syndrome I RMS003
Rapadilino Syndrome RPD002
Raph Blood Group System RPH001
Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome RPD006
Rapidly Involuting Congenital Hemangioma RPD005
Rapidly Progressive Glomerulonephritis RPD001
Rapp-Hodgkin Syndrome RPP001 EDRH
Rare Adenocarcinoma of the Breast RRD004
Rare Idiopathic Male Infertility RRD006
Rare Intellectual Disability Without Developmental Anomaly RRN002
Rare Isolated Myopia RRS002
Rare Lichen Planus RRL001
Rare Variants of Adenocarcinoma of the Corpus Uteri RRV001
Ras-Associated Autoimmune Leukoproliferative Disorder RSS025
Rasa1-Related Disorders RS1001
Rasmussen Encephalitis RSM001
Rasmussen Johnsen Thomsen Syndrome RSM002
Rasmussen Subacute Encephalitis RSM003
Rat Bite Fever RTB001
Ravine Syndrome RVN001
Raynaud Disease RYN001
Raynaud Phenomenon RYN005
Reactive Angioendotheliomatosis RCT024
Reactive Arthritis RCT015
Reading Disorder RDN001
Reardon Wilson Cavanagh Syndrome RRD001
Recessive Dystrophic Epidermolysis Bullosa RCS002
Recessive Dystrophic Epidermolysis Bullosa-Generalized Other RCS008
Recessive Intellectual Disability-Motor Dysfunction-Multiple Joint Contractures Syndrome RCS010
Recombinant 8 Syndrome RCM004
Recombinant Chromosome 8 Syndrome RCM003
Recombinase Activating Gene 1 Deficiency RCM002
Recombinase Activating Gene 2 Deficiency RCM001
Recombination Rate Quantitative Trait Locus 1 RCM006
Rectal Cancer, Childhood RCT025
Rectal Cloacogenic Carcinoma RCT007
Rectal Disease RCT017
Rectal Duplication RCT033
Rectal Neoplasm RCT018
Rectosigmoid Junction Neoplasm RCT008
Rectum Adenocarcinoma RCT020
Rectum Adenoma RCT035
Rectum Carcinoma in Situ RCT010
Rectum Kaposi's Sarcoma RCT014
Rectum Leiomyoma RCT004
Rectum Leiomyosarcoma RCT016
Rectum Lymphoma RCT002
Rectum Malignant Melanoma RCT003
Rectum Mucinous Adenocarcinoma RCT006
Rectum Neuroendocrine Neoplasm RCT005
Rectum Rhabdomyosarcoma RCT012
Rectum Sarcoma RCT022
Rectum Sarcomatoid Carcinoma RCT001
Rectum Signet Ring Adenocarcinoma RCT013
Rectum Squamous Cell Carcinoma RCT023
Recurrent Acute Pancreatitis RCR022
Recurrent Corneal Erosion RCR001
Recurrent Hepatitis C Virus Induced Liver Disease in Liver Transplant Recipients RCR023
Recurrent Hydatidiform Mole RCR026
Recurrent Hypersomnia RCR002
Recurrent Idiopathic Neuroretinitis RCR030
Recurrent Peripheral Facial Palsy RCR003
Recurrent Respiratory Papillomatosis RCR004
Red Cell Permeability Defect RDC013
Red Cell Phospholipid Defect with Hemolysis RDC003
Red Skin Pigment Anomaly of New Guinea RDS002
Red-Green Color Blindness RDG001
Reducing Body Myopathy RDC010
Reducing Body Myopathy, X-Linked 1a, Severe, with Infantile or Early Childhood Onset RDC016
Reducing Body Myopathy, X-Linked 1b, with Late Childhood or Adult Onset RDC012
Reductional Transverse Limb Defects RDC004
Reese Retinal Dysplasia RSR001
Reflex Epilepsy RFL002
Reflex Sympathetic Dystrophy RFL001
Refractive Error RFR003
Refractory Anemia RFR010
Refractory Anemia with Excess Blasts RFR008
Refractory Anemia with Excess Blasts in Transformation RFR007
Refractory Anemia with Excess Blasts Type 1 RFR015
Refractory Anemia with Excess Blasts Type 2 RFR014
Refractory Celiac Disease RFR013
Refractory Cytopenia with Unilineage Dysplasia RFR006
Refractory Hairy Cell Leukemia RFR002
Refractory Hematologic Cancer RFR004
Refractory Plasma Cell Neoplasm RFR001
Refsum Disease with Increased Pipecolic Acidemia RFS002
Refsum Disease, Classic RFS006
Refsum Disease, Infantile Form RFS003
Reginato Shiapachasse Syndrome RGN002
Regional Odontodysplasia RGN005
Regional Ureteric Cancer RGN001
Regressive Spondylometaphyseal Dysplasia RGR003
Regular Astigmatism RGL001
Relapsed/refractory Diffuse Large B-Cell Lymphoma RLP008
Relapsing Epidemic Typhus RLP007
Relapsing Fever RLP003
Relapsing Polychondritis RLP001
Relapsing-Remitting Multiple Sclerosis RLP002
Rem Sleep Behavior Disorder RMS001
Ren-Related Kidney Disease RNR002
Renal Adenoma RNL013
Renal Adysplasia Dominant Type RNL030
Renal Agenesis Meningomyelocele Mullerian Defect RNL031
Renal Agenesis, Bilateral RNL123
Renal and Mullerian Duct Hypoplasia RNL116
Renal Artery Atheroma RNL008
Renal Artery Disease RNL097
Renal Artery Obstruction RNL001
Renal Caliceal Diverticuli Deafness RNL032
Renal Carcinoma, Familial RNL033
Renal Cell Carcinoma 4 RNL034
Renal Cell Carcinoma Associated with Neuroblastoma RNL088
Renal Cell Carcinoma, Nonpapillary RNL114
Renal Cell Carcinoma, Papillary, 1 RNL065
Renal Cell Carcinoma, Xp11-Associated RNL119
Renal Cysts and Diabetes Syndrome RNL051
Renal Dysplasia RNL078
Renal Dysplasia Diffuse Autosomal Recessive RNL035
Renal Dysplasia Diffuse Cystic RNL036
Renal Dysplasia-Limb Defects Syndrome RNL039
Renal Dysplasia, Bilateral RNL107
Renal Dysplasia, Cystic RNL094
Renal Dysplasia, Unilateral RNL106
Renal Failure, Progressive, with Hypertension RNL113
Renal Fibrosis RNL077
Renal Glucosuria RNL024
Renal Hypertension RNL015
Renal Hypodysplasia/aplasia 1 RNL100
Renal Hypodysplasia/aplasia 2 RNL099
Renal Hypodysplasia/aplasia 3 RNL122
Renal Hypoplasia RNL025
Renal Hypoplasia, Bilateral RNL109
Renal Hypoplasia, Unilateral RNL108
Renal Infectious Disease RNL016
Renal Nutcracker Syndrome RNL089
Renal Oncocytoma RNL017
Renal Osteodystrophy RNL011
Renal Pelvis Adenocarcinoma RNL004
Renal Pelvis Carcinoma RNL018
Renal Pelvis Inverted Papilloma RNL010
Renal Pelvis Squamous Cell Carcinoma RNL009
Renal Pelvis Transitional Cell Carcinoma RNL019
Renal Pelvis Urothelial Papilloma RNL020
Renal Tuberculosis RNL012
Renal Tubular Acidosis RNL007
Renal Tubular Acidosis Iii RNL117
Renal Tubular Acidosis, Distal RNL045
Renal Tubular Acidosis, Distal, Autosomal Dominant RNL046
Renal Tubular Acidosis, Distal, Autosomal Recessive RNL047
Renal Tubular Acidosis, Distal, Type 3 RNL048
Renal Tubular Acidosis, Distal, Type 4 RNL049
Renal Tubular Acidosis, Distal, with Hemolytic Anemia RNL054
Renal Tubular Acidosis, Distal, with Nephrocalcinosis, Short Stature, Mental Retardation, and Distinctive Facies RNL121
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness RNL118
Renal Tubular Acidosis, Proximal RNL115
Renal Tubular Acidosis, Proximal, with Ocular Abnormalities and Mental Retardation RNL120
Renal Tubular Dysgenesis RNL028
Renal Tubular Dysgenesis Due to Twin-Twin Transfusion RNL090
Renal Tubular Transport Disease RNL021
Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia RNL111
Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia Due to Duplication of Mitochondrial Dna RNL050
Renal-Hepatic-Pancreatic Dysplasia RNL059
Renal-Hepatic-Pancreatic Dysplasia 1 RNL092
Renal-Hepatic-Pancreatic Dysplasia 2 RNL095
Renal, Genital, and Middle Ear Anomalies RNL112
Renier Gabreels Jasper Syndrome RNR001
Renoanogenital Syndrome RNN001
Renoprival Hypertension RNP002
Renovascular Hypertension RNV001
Renpenning Syndrome 1 RNP003
Repetitive Motion Disorders RPT005
Repetitive Stress Injuries RPT006
Repressor of Telomerase Expression 1 RPR004
Reproductive Organ Benign Neoplasm RPR001
Reproductive System Disease RPR002
Residual Stage Angle-Closure Glaucoma RSD001
Residual Stage Corticosteroid-Induced Glaucoma RSD003
Residual Stage of Open Angle Glaucoma RSD002
Resistance to Bleomycine in the Treatment of Testicular Cancer RSS021
Resistance to Lh RSS003
Resistance to Tamoxifene RSS022
Resistance to Thyrotropin-Releasing Hormone Syndrome RSS007
Resistance to Vitamin K Antagonists RSS024
Respiratory Bronchiolitis-Interstitial Lung Disease Syndrome RSP018
Respiratory Distress Syndrome in Premature Infants RSP019
Respiratory Distress Syndrome, Infant RSP007
Respiratory Failure RSP003
Respiratory Rhythmicity in Sleep RSP008
Respiratory Syncytial Virus Infectious Disease RSP002
Respiratory System Benign Neoplasm RSP004
Respiratory System Cancer RSP005
Respiratory System Disease RSP006
Respiratory Underresponsiveness to Hypoxia and Hypercapnia RSP020
Resting Heart Rate, Variation in RST023
Restless Legs Syndrome RST001
Restless Legs Syndrome 1 RST012 RLS1
Restless Legs Syndrome 2 RST013
Restless Legs Syndrome 3 RST014
Restless Legs Syndrome 4 RST015
Restless Legs Syndrome 5 RST021
Restless Legs Syndrome 6 RST020
Restless Legs Syndrome 7 RST016
Restless Legs Syndrome 8 RST019
Restrictive Cardiomyopathy RST002
Restrictive Dermopathy, Lethal RST011
Rete Ovarii Adenocarcinoma RTV002
Rete Ovarii Adenoma RTV004
Rete Ovarii Cystadenofibroma RTV003
Rete Ovarii Cystadenoma RTV001
Rete Ovarii Neoplasm RTV005
Rete Testis Adenocarcinoma RTT004
Rete Testis Adenoma RTT003
Rete Testis Neoplasm RTT005
Reticular Dysgenesis RTC002
Reticular Dystrophy of Retinal Pigment Epithelium RTC011
Reticular Pattern Testicular Yolk Sac Tumor RTC004
Reticular Perineurioma RTC007
Reticulate Acropigmentation of Kitamura RTC008
Reticuloendotheliosis RTC010
Reticuloendotheliosis, X-Linked RTC012
Reticulohistiocytic Granuloma RTC001
Reticulosarcoma RTC005
Reticulum Cell Sarcoma RTC009
Retiform Hemangioendothelioma RTF001
Retina Lymphoma RTN011
Retinal Aplasia RTN198
Retinal Arterial Macroaneurysm with Supravalvular Pulmonic Stenosis RTN145
Retinal Arteries, Tortuosity of RTN179
Retinal Artery Occlusion RTN014
Retinal Cancer RTN015
Retinal Capillary Malformation RTN189
Retinal Cone Dystrophy 1 RTN032
Retinal Cone Dystrophy 3a RTN034
Retinal Cone Dystrophy 3b RTN035
Retinal Cone Dystrophy 4 RTN036
Retinal Degeneration RTN016
Retinal Degeneration and Epilepsy RTN202
Retinal Degeneration with Nanophthalmos, Cystic Macular Degeneration, and Angle Closure Glaucoma RTN037
Retinal Detachment RTN017
Retinal Disease RTN018
Retinal Drusen RTN006
Retinal Dysplasia X-Linked RTN038
Retinal Dysplasia, Primary RTN185
Retinal Dystrophies Primarily Involving Bruch's Membrane RTN009
Retinal Dystrophy and Iris Coloboma with or Without Congenital Cataract RTN211
Retinal Dystrophy and Obesity RTN173
Retinal Dystrophy in Systemic or Cerebroretinal Lipidoses RTN007
Retinal Dystrophy with Inner Retinal Dysfunction and Ganglion Cell Abnormalities RTN170
Retinal Dystrophy with or Without Extraocular Anomalies RTN191
Retinal Dystrophy with or Without Macular Staphyloma RTN212
Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome RTN135
Retinal Dystrophy, Juvenile Cataracts, and Short Stature Syndrome RTN174
Retinal Dystrophy, Reticular Pigmentary, of Posterior Pole RTN203
Retinal Hemangioblastoma RTN013
Retinal Ischemia RTN003
Retinal Lattice Degeneration RTN005
Retinal Melanoma RTN010
Retinal Microaneurysm RTN004
Retinal Perforation RTN002
Retinal Telangiectasia RTN019
Retinal Telangiectasia and Hypogammaglobulinemia RTN204
Retinal Vascular Disease RTN020
Retinal Vascular Occlusion RTN021
Retinal Vasculitis RTN001
Retinal Vein Occlusion RTN022
Retinal Venous Beading RTN199
Retinis Pigmentosa Deafness Hypogenitalism RTN040
Retinitis RTN023
Retinitis Pigmentosa RTN008
Retinitis Pigmentosa 1 RTN172
Retinitis Pigmentosa 10 RTN150
Retinitis Pigmentosa 11 RTN041
Retinitis Pigmentosa 12 RTN042
Retinitis Pigmentosa 13 RTN043
Retinitis Pigmentosa 14 RTN044
Retinitis Pigmentosa 17 RTN046
Retinitis Pigmentosa 18 RTN047
Retinitis Pigmentosa 19 RTN048
Retinitis Pigmentosa 2 RTN162
Retinitis Pigmentosa 2, X-Linked RTN181
Retinitis Pigmentosa 20 RTN050
Retinitis Pigmentosa 22 RTN051
Retinitis Pigmentosa 23 RTN052
Retinitis Pigmentosa 24 RTN053
Retinitis Pigmentosa 25 RTN054
Retinitis Pigmentosa 26 RTN055
Retinitis Pigmentosa 27 RTN131
Retinitis Pigmentosa 28 RTN056
Retinitis Pigmentosa 29 RTN057
Retinitis Pigmentosa 3 RTN058
Retinitis Pigmentosa 30 RTN059
Retinitis Pigmentosa 31 RTN060
Retinitis Pigmentosa 32 RTN061
Retinitis Pigmentosa 33 RTN062
Retinitis Pigmentosa 34 RTN063
Retinitis Pigmentosa 35 RTN064
Retinitis Pigmentosa 36 RTN065
Retinitis Pigmentosa 37 RTN157
Retinitis Pigmentosa 38 RTN142
Retinitis Pigmentosa 39 RTN141
Retinitis Pigmentosa 4 RTN066
Retinitis Pigmentosa 40 RTN134
Retinitis Pigmentosa 41 RTN067
Retinitis Pigmentosa 42 RTN149
Retinitis Pigmentosa 43 RTN133
Retinitis Pigmentosa 44 RTN136
Retinitis Pigmentosa 45 RTN159
Retinitis Pigmentosa 46 RTN130
Retinitis Pigmentosa 47 RTN143
Retinitis Pigmentosa 48 RTN147
Retinitis Pigmentosa 49 RTN129
Retinitis Pigmentosa 50 RTN210
Retinitis Pigmentosa 51 RTN106
Retinitis Pigmentosa 54 RTN085
Retinitis Pigmentosa 55 RTN090
Retinitis Pigmentosa 56 RTN116
Retinitis Pigmentosa 57 RTN117
Retinitis Pigmentosa 58 RTN114
Retinitis Pigmentosa 59 RTN171
Retinitis Pigmentosa 6 RTN068
Retinitis Pigmentosa 60 RTN160
Retinitis Pigmentosa 61 RTN144
Retinitis Pigmentosa 62 RTN146
Retinitis Pigmentosa 63 RTN148
Retinitis Pigmentosa 66 RTN152
Retinitis Pigmentosa 67 RTN140
Retinitis Pigmentosa 68 RTN165
Retinitis Pigmentosa 69 RTN166
Retinitis Pigmentosa 7 RTN069
Retinitis Pigmentosa 70 RTN169
Retinitis Pigmentosa 71 RTN176
Retinitis Pigmentosa 72 RTN178
Retinitis Pigmentosa 73 RTN177
Retinitis Pigmentosa 74 RTN180
Retinitis Pigmentosa 75 RTN186
Retinitis Pigmentosa 76 RTN190
Retinitis Pigmentosa 77 RTN192
Retinitis Pigmentosa 78 RTN196
Retinitis Pigmentosa 79 RTN195
Retinitis Pigmentosa 80 RTN213
Retinitis Pigmentosa 81 RTN214
Retinitis Pigmentosa 9 RTN070
Retinitis Pigmentosa and Erythrocytic Microcytosis RTN193
Retinitis Pigmentosa Inversa with Deafness RTN205
Retinitis Pigmentosa with or Without Situs Inversus RTN158
Retinitis Pigmentosa with or Without Skeletal Anomalies RTN194
Retinitis Pigmentosa-Deafness Syndrome RTN187
Retinitis Pigmentosa-Intellectual Disability-Deafness-Hypogonadism Syndrome RTN215
Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism RTN071
Retinitis Pigmentosa, Late-Adult Onset RTN206
Retinitis Pigmentosa, X-Linked, and Sinorespiratory Infections, with or Without Deafness RTN104
Retinitis Pigmentosa, Y-Linked RTN102
Retinoblastoma RTN024
Retinochoroidal Coloboma RTN123
Retinohepatoendocrinologic Syndrome RTN072
Retinopathy Anemia Cns Anomalies RTN073
Retinopathy Aplastic Anemia Neurological Abnormalities RTN074
Retinopathy, Arteriosclerotic RTN076
Retinopathy, Pericentral Pigmentary, Autosomal Recessive RTN208
Retinopathy, Pericentral Pigmentary, Dominant RTN200
Retinopathy, Pigmentary, and Mental Retardation RTN207
Retinoschisis 1, X-Linked, Juvenile RTN209
Retinoschisis of Fovea RTN078
Retinoschisis, Autosomal Dominant RTN201
Retrocerebellar Cyst RTR022
Retrograde Amnesia RTR001
Retromolar Area Cancer RTR002
Retroperitoneal Fibrosis RTR011
Retroperitoneal Germ Cell Neoplasm RTR003
Retroperitoneal Hemangiopericytoma RTR006
Retroperitoneal Leiomyosarcoma RTR007
Retroperitoneal Liposarcoma RTR012
Retroperitoneal Lymphoma RTR005
Retroperitoneal Neuroblastoma RTR023
Retroperitoneal Sarcoma RTR010
Retroperitoneum Carcinoma RTR004
Retrovirus-Associated Myelopathy RTR017
Rett Syndrome RTT002
Rett Syndrome, Congenital Variant RTT008
Reunion Island Larsen Syndrome RNN006
Reversible Cerebral Vasoconstriction Syndrome RVR002
Revesz Syndrome RVS001
Reye Syndrome RYS001
Reynolds Neri Hermann Syndrome RYN002
Reynolds Syndrome RYN003
Rh Isoimmunization RHS001
Rh-Null, Amorph Type RHN014
Rh-Null, Regulator Type RHN013
Rhabditida Infections RHB006
Rhabdoid Cancer RHB001
Rhabdoid Meningioma RHB002
Rhabdoid Tumor Predisposition Syndrome 1 RHB008
Rhabdoid Tumor Predisposition Syndrome 2 RHB011
Rhabdomyomatous Mesenchymal Hamartoma RHB007
Rhabdomyosarcoma RHB003
Rhabdomyosarcoma 2 RHB024
Rhabdomyosarcoma of the Cervix Uteri RHB019
Rhabdomyosarcoma of the Corpus Uteri RHB018
Rhabdomyosarcoma, Embryonal, 1 RHB023
Rhabdomyosarcoma, Embryonal, 2 RHB021
Rheumatic Disease RHM027
Rheumatic Encephalitis RHM016
Rheumatic Fever RHM001
Rheumatic Fever-Related Antigen RHM035
Rheumatic Heart Disease RHM028
Rheumatic Myocarditis RHM008
Rheumatic Pulmonary Valve Disease RHM002
Rheumatoid Arthritis RHM011
Rheumatoid Arthritis, Systemic Juvenile RHM021
Rheumatoid Factor-Negative Juvenile Idiopathic Arthritis RHM032
Rheumatoid Factor-Negative Juvenile Idiopathic Arthritis with Anti-Nuclear Antibodies RHM031
Rheumatoid Factor-Negative Juvenile Idiopathic Arthritis Without Anti-Nuclear Antibodies RHM030
Rheumatoid Factor-Positive Polyarticular Juvenile Idiopathic Arthritis RHM033
Rheumatoid Lung Disease RHM009
Rheumatoid Nodulosis RHM013
Rheumatoid Vasculitis RHM014
Rhinitis RHN004
Rhinoscleroma RHN002
Rhinosporidiosis RHN003
Rhiny RHN012
Rhizomelic Chondrodysplasia Punctata RHZ001
Rhizomelic Chondrodysplasia Punctata, Type 1 RHZ011
Rhizomelic Chondrodysplasia Punctata, Type 2 RHZ014
Rhizomelic Chondrodysplasia Punctata, Type 3 RHZ004
Rhizomelic Chondrodysplasia Punctata, Type 5 RHZ015
Rhizomelic Dysplasia, Patterson-Lowry Type RHZ012
Rhizomelic Dysplasia, Scoliosis, and Retinitis Pigmentosa RHZ006
Rhizomelic Pseudopolyarthritis RHZ007
Rhizomelic Syndrome RHZ008
Rhombencephalosynapsis RHM015
Rhyns Syndrome RHY001
Ribbing Disease RBB001
Riboflavin Deficiency RBF001
Riboflavin Transporter Deficiency RBF003
Riboflavin Transporter Deficiency Neuronopathy RBF002
Ribose 5-Phosphate Isomerase Deficiency RBS005
Richards-Rundle Syndrome RCH002
Richieri Costa Da Silva Syndrome RCH003
Richieri Costa Orquizas Syndrome RCH005
Richieri-Costa Colletto Otto Syndrome RCH007
Richieri-Costa Guion-Almeida Cohen Syndrome RCH008
Richieri-Costa/guion-Almeida Syndrome RCH010
Richter's Syndrome RCH001
Rickets RCK004
Rickettsia Parkeri Spotted Fever RCK001
Rickettsialpox RCK003
Riddle Syndrome RDD003
Riedel's Fibrosing Thyroiditis RDL003
Rift Valley Fever RFT001
Right Aortic Arch RGH006
Right Atrial Isomerism RGH009
Right Atrium Familial Dilatation RGH002
Right Bundle Branch Block RGH001
Right Inferior Vena Cava Connecting to Left-Sided Atrium RGH007
Right Pulmonary Artery, Anomalous Origin of, Familial RGH011
Right Superior Vena Cava Connecting to Left-Sided Atrium RGH008
Right Ventricle Hypoplasia RGH003
Right Ventricular Hypoplasia, Isolated RGH010
Rigid Spine Muscular Dystrophy 1 RGD003
Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal RGD002
Ring Chromosome 1 RNG004
Ring Chromosome 10 RNG005
Ring Chromosome 11 RNG006
Ring Chromosome 12 RNG007
Ring Chromosome 13 RNG008
Ring Chromosome 14 Syndrome RNG029
Ring Chromosome 15 RNG010
Ring Chromosome 16 RNG011
Ring Chromosome 17 RNG012
Ring Chromosome 18 RNG013
Ring Chromosome 19 RNG014
Ring Chromosome 2 RNG015
Ring Chromosome 20 RNG016
Ring Chromosome 21 RNG017
Ring Chromosome 22 RNG018
Ring Chromosome 3 RNG019
Ring Chromosome 4 RNG020
Ring Chromosome 5 RNG021
Ring Chromosome 6 RNG022
Ring Chromosome 7 RNG023
Ring Chromosome 8 RNG024
Ring Chromosome 9 RNG025
Ring Chromosome Y Syndrome RNG031
Ring Corneal Ulcer RNG002
Ring Dermoid of Cornea RNG003
Ring Staphyloma RNG001
Ringed Hair RNG030
Rippling Muscle Disease 1 RPP007
Rippling Muscle Disease 2 RPP006
Rippling Muscle Disease with Myasthenia Gravis RPP004
Ritscher-Schinzel Syndrome RTS001
Ritscher-Schinzel Syndrome 1 RTS003
Ritscher-Schinzel Syndrome 2 RTS002
Ritter's Disease RTT001
Rnase T2-Deficient Leukoencephalopathy RNS005
Roberts Syndrome RBR001
Robin Sequence with Cleft Mandible and Limb Anomalies RBN014
Robin Sequence with Distinctive Facial Appearance and Brachydactyly RBN019
Robinow Syndrome RBN002
Robinow Syndrome, Autosomal Dominant 1 RBN018
Robinow Syndrome, Autosomal Dominant 2 RBN017
Robinow Syndrome, Autosomal Dominant 3 RBN020
Robinow Syndrome, Autosomal Recessive RBN009
Robinow-Like Syndrome RBN010
Robinow-Sorauf Syndrome RBN013
Roch-Leri Mesosomatous Lipomatosis RCH009
Rocky Mountain Spotted Fever RCK002
Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction RDC015
Rodini Richieri Costa Syndrome RDN002
Rodrigues Blindness RDR002
Rohhad RHH001
Roifman Syndrome RFM001
Roifman-Chitayat Syndrome RFM002
Rokitansky Sequence RKT002
Rokitansky-Aschoff Sinuses of the Gallbladder RKT003
Rolandic Epilepsy-Speech Dyspraxia Syndrome RLN004
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked RLN001
Rombo Syndrome RMB001
Rommen Mueller Sybert Syndrome RMM001
Root Caries RTC003
Root Resorption RTR008
Ror2-Related Robinow Syndrome RR2001
Rosacea RSC001
Rosacea Conjunctivitis RSC002
Rosai-Dorfman Disease RSD004
Rosette-Forming Glioneuronal Tumor RST024
Ross River Fever RSS001
Rosselli-Gulienetti Syndrome RSS006
Rothmund-Thomson Syndrome RTH001
Rothmund-Thomson Syndrome Type 1 RTH004
Rothmund-Thomson Syndrome Type 2 RTH005
Round Ligament Malignant Neoplasm RND001
Roussy-Levy Hereditary Areflexic Dystasia RSS026
Rowley-Rosenberg Syndrome RWL001
Roy Maroteaux Kremp Syndrome RYM001
Rozin Hertz Goodman Syndrome RZN001
Rrm2b-Related Mitochondrial Disease RRM002
Rrm2b-Related Mitochondrial Dna Depletion Syndrome RRM004
Rrm2b-Related Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form with Renal Tubulopathy RRM005
Rubella RBL001
Rubella Panencephalitis RBL002
Rubeosis Iridis RBS002
Rubinstein Taybi Like Syndrome RBN007
Rubinstein-Taybi Syndrome 1 RBN021
Rubinstein-Taybi Syndrome 2 RBN008
Rud Syndrome RDS004
Rudiger Syndrome RDG003
Ruijs-Aalfs Syndrome RJS001
Rumination Disorder RMN001
Russell-Silver Syndrome, X-Linked RSS027
Rutherfurd Syndrome RTH002
Ruvalcaba Churesigaew Myhre Syndrome RVL001
Ruvalcaba Syndrome RVL002
Ruzicka Goerz Anton Syndrome RZC001
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