Disease Name Symbol Acronym
Rab18 Deficiency RB1001
Rabies RBS001 LYSSA
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 RRDX
Radial Ray Hypoplasia with Choanal Atresia RDL029
Radial-Renal Syndrome RDL030
Radiation Cystitis RDT001
Radiation Induced Angiosarcoma of the Breast RDT003 RIA
Radiation Induced Brachial Plexopathy RDT004
Radiation Induced Cancer RDT005
Radiation Myelitis RDT014
Radiation Proctitis RDT013
Radiation Sensitivity of Natural Killer Activity RDT015 XNKS
Radiation Sensitivity/chromosome Instability Syndrome, Autosomal Dominant RDT007
Radiation-Induced Plexopathy RDT016
Radiculoneuropathy, Fatal Neonatal RDC014
Radiculopathy RDC002
Radin Blood Group Antigen RDN004 RD
Radio Renal Syndrome RDR001
Radio-Digito-Facial Dysplasia RDD001
Radiohumeral Fusions with Other Skeletal and Craniofacial Anomalies RDH004 RHFCA
Radioulnar Synostosis RDL002
Radio-Ulnar Synostosis Type 1 RDL012
Radio-Ulnar Synostosis Type 2 RDL013
Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia 1 RDL034 RUSAT1
Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia 2 RDL033 RUSAT2
Radioulnar Synostosis with Microcephaly, Short Stature, Scoliosis, and Mental Retardation RDL014
Radio-Ulnar Synostosis, Bilateral RDL020
Radioulnar Synostosis, Radial Ray Abnormalities, and Severe Malformations in the Male RDL036
Radio-Ulnar Synostosis, Unilateral RDL019
Radioulnar Synostosis, Unilateral, with Developmental Retardation and Hypotonia RDL032
Radio-Ulnar Synostosis-Amegakaryocytic Thrombocytopenia Syndrome RDL039
Radioulnar Synostosis-Microcephaly-Scoliosis Syndrome RDL026
Radius Absent Anogenital Anomalies RDS001
Radius, Aplasia of, with Cleft Lip/palate RDS005
Ragweed Sensitivity RGW001
Rahman Syndrome RHM034 RMNS
Rainbow Trout Allergy RNB001
Raindrop Hypopigmentation RND003
Raine Syndrome RNS001 RNS
Rajab Syndrome RJB001
Raltegravir Toxicity RLT001
Ramer Ladda Syndrome RMR001 HRS
Ramon Syndrome RMN002
Ramos Arroyo Clark Syndrome RMS002
Ramsay Hunt Syndrome I RMS003
Ranitidine Allergy RNT001
Rapadilino Syndrome RPD002 RAPADILINOS
Raph Blood Group System RPH001 MER2
Rapidly Involuting Congenital Hemangioma RPD005 RICH
Rapidly Progressive Glomerulonephritis RPD001 RPGN
Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome RPD006
Rapp-Hodgkin Syndrome RPP001 OFC8
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
Rasa1-Related Disorders RS1001
Ras-Associated Autoimmune Leukoproliferative Disorder RSS025 RALD
Rasmussen Encephalitis RSM001 RE
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 RAE
Reactive Arthritis RCT015 PIRA
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 IDMDC
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 FRHM
Recurrent Hypersomnia RCR002
Recurrent Idiopathic Neuroretinitis RCR030 RINR
Recurrent Peripheral Facial Palsy RCR003
Recurrent Respiratory Papillomatosis RCR004 RRP
Red Cell Permeability Defect RDC013
Red Cell Phospholipid Defect with Hemolysis RDC003 HPCHA
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 RBMX1A
Reducing Body Myopathy, X-Linked 1b, with Late Childhood or Adult Onset RDC012 RBMX1B
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 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 RCUD
Refractory Hairy Cell Leukemia RFR002
Refractory Hematologic Cancer RFR004
Refractory Plasma Cell Neoplasm RFR001
Refsum Disease with Increased Pipecolic Acidemia RFS002 RDPA
Refsum Disease, Classic RFS006 RD
Refsum Disease, Infantile Form RFS003 IRD
Reginato Shiapachasse Syndrome RGN002
Regional Odontodysplasia RGN005
Regional Ureteric Cancer RGN001
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 RRMS
Rem Sleep Behavior Disorder RMS001
Remazole Black Respiratory Allergy RMZ001
Remitting Seronegative Symmetrical Synovitis with Pitting Edema RMT001
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 RCC4
Renal Cell Carcinoma Associated with Neuroblastoma RNL088
Renal Cell Carcinoma, Nonpapillary RNL114 RCC
Renal Cell Carcinoma, Papillary, 1 RNL065 RCCP
Renal Cell Carcinoma, Xp11-Associated RNL119 RCCX1
Renal Cysts and Diabetes Syndrome RNL051 RCAD
Renal Dysplasia RNL078
Renal Dysplasia Diffuse Autosomal Recessive RNL035
Renal Dysplasia Diffuse Cystic RNL036
Renal Dysplasia, Bilateral RNL107
Renal Dysplasia, Cystic RNL094 CYSRD
Renal Dysplasia, Unilateral RNL106
Renal Dysplasia-Limb Defects Syndrome RNL039
Renal Failure, Progressive, with Hypertension RNL113 AORF
Renal Fibrosis RNL077
Renal Glucosuria RNL024 GLYS
Renal Hypertension RNL015
Renal Hypodysplasia/aplasia 1 RNL100 RHDA1
Renal Hypodysplasia/aplasia 2 RNL099 RHDA2
Renal Hypodysplasia/aplasia 3 RNL122 RHDA3
Renal Hypoplasia RNL025
Renal Hypoplasia, Bilateral RNL109
Renal Hypoplasia, Unilateral RNL108
Renal Infectious Disease RNL016
Renal Nutcracker Syndrome RNL089 RNS
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 DRTA
Renal Tubular Acidosis, Distal, Autosomal Dominant RNL046 AD-DRTA
Renal Tubular Acidosis, Distal, Autosomal Recessive RNL047 RTADR
Renal Tubular Acidosis, Distal, Type 3 RNL048
Renal Tubular Acidosis, Distal, Type 4 RNL049
Renal Tubular Acidosis, Distal, with Hemolytic Anemia RNL054 DRTA-HA
Renal Tubular Acidosis, Distal, with Nephrocalcinosis, Short Stature, Mental Retardation, and Distinctive Facies RNL121
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness RNL118 DRTA-D
Renal Tubular Acidosis, Proximal RNL115 PRTA
Renal Tubular Acidosis, Proximal, with Ocular Abnormalities and Mental Retardation RNL120 PRTA-OA
Renal Tubular Dysgenesis RNL028 RTD
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, Genital, and Middle Ear Anomalies RNL112
Renal-Hepatic-Pancreatic Dysplasia RNL059
Renal-Hepatic-Pancreatic Dysplasia 1 RNL092 RHPD1
Renal-Hepatic-Pancreatic Dysplasia 2 RNL095 RHPD2
Renier Gabreels Jasper Syndrome RNR001
Renoanogenital Syndrome RNN001
Renoprival Hypertension RNP002
Renovascular Hypertension RNV001
Renpenning Syndrome 1 RNP003 RENS1
Ren-Related Kidney Disease RNR002
Repetitive Motion Disorders RPT005
Repetitive Stress Injuries RPT006
Repressor of Telomerase Expression 1 RPR004 RTE1
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 Allergy RSP021
Respiratory Bronchiolitis-Interstitial Lung Disease Syndrome RSP018
Respiratory Distress Syndrome in Premature Infants RSP019 RDS
Respiratory Distress Syndrome, Infant RSP007 IRDS
Respiratory Failure RSP003
Respiratory Rhythmicity in Sleep RSP008 RRIS
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 RHR
Restless Legs Syndrome RST001 RLS
Restless Legs Syndrome 1 RST012 RLS1
Restless Legs Syndrome 2 RST013 RLS2
Restless Legs Syndrome 3 RST014 RLS3
Restless Legs Syndrome 4 RST015 RLS4
Restless Legs Syndrome 5 RST021 RLS5
Restless Legs Syndrome 6 RST020 RLS6
Restless Legs Syndrome 7 RST016 RLS7
Restless Legs Syndrome 8 RST019 RLS8
Restrictive Cardiomyopathy RST002 RCM
Restrictive Dermopathy, Lethal RST011 LTSCS
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 RDYS
Reticular Dystrophy of Retinal Pigment Epithelium RTC011
Reticular Pattern Testicular Yolk Sac Tumor RTC004
Reticular Perineurioma RTC007
Reticulate Acropigmentation of Kitamura RTC008 RAK
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 RAMSVPS
Retinal Arteries, Tortuosity of RTN179 RATOR
Retinal Artery Occlusion RTN014
Retinal Cancer RTN015
Retinal Capillary Malformation RTN189
Retinal Cone Dystrophy 1 RTN032 RCD1
Retinal Cone Dystrophy 3a RTN034 RCD3A
Retinal Cone Dystrophy 3b RTN035 RCD3B
Retinal Cone Dystrophy 4 RTN036 RCD4
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 PRD
Retinal Dystrophies Primarily Involving Bruch's Membrane RTN009
Retinal Dystrophy and Iris Coloboma with or Without Congenital Cataract RTN211 RDICC
Retinal Dystrophy and Obesity RTN173 RDOB
Retinal Dystrophy in Systemic or Cerebroretinal Lipidoses RTN007
Retinal Dystrophy with Inner Retinal Dysfunction and Ganglion Cell Abnormalities RTN170 RDGCA
Retinal Dystrophy with or Without Extraocular Anomalies RTN191 RDEOA
Retinal Dystrophy with or Without Macular Staphyloma RTN212 RDMS
Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome RTN135 RDCCAS
Retinal Dystrophy, Juvenile Cataracts, and Short Stature Syndrome RTN174 RDJCSS
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 RP
Retinitis Pigmentosa 1 RTN172 RP1
Retinitis Pigmentosa 10 RTN150 RP10
Retinitis Pigmentosa 11 RTN041 RP11
Retinitis Pigmentosa 12 RTN042 RP12
Retinitis Pigmentosa 13 RTN043 RP13
Retinitis Pigmentosa 14 RTN044 RP14
Retinitis Pigmentosa 17 RTN046 RP17
Retinitis Pigmentosa 18 RTN047 RP18
Retinitis Pigmentosa 19 RTN048 RP19
Retinitis Pigmentosa 2 RTN162 RP2
Retinitis Pigmentosa 2, X-Linked RTN181 RP 2
Retinitis Pigmentosa 20 RTN050 RP20
Retinitis Pigmentosa 22 RTN051 RP22
Retinitis Pigmentosa 23 RTN052 RP23
Retinitis Pigmentosa 24 RTN053 RP24
Retinitis Pigmentosa 25 RTN054 RP25
Retinitis Pigmentosa 26 RTN055 RP26
Retinitis Pigmentosa 27 RTN131 RP27
Retinitis Pigmentosa 28 RTN056 RP28
Retinitis Pigmentosa 29 RTN057 RP29
Retinitis Pigmentosa 3 RTN058 RP3
Retinitis Pigmentosa 30 RTN059 RP30
Retinitis Pigmentosa 31 RTN060 RP31
Retinitis Pigmentosa 32 RTN061 RP32
Retinitis Pigmentosa 33 RTN062 RP33
Retinitis Pigmentosa 34 RTN063 RP34
Retinitis Pigmentosa 35 RTN064 RP35
Retinitis Pigmentosa 36 RTN065 RP36
Retinitis Pigmentosa 37 RTN157 RP37
Retinitis Pigmentosa 38 RTN142 RP38
Retinitis Pigmentosa 39 RTN141 RP39
Retinitis Pigmentosa 4 RTN066 RP4
Retinitis Pigmentosa 40 RTN134 RP40
Retinitis Pigmentosa 41 RTN067 RP41
Retinitis Pigmentosa 42 RTN149 RP42
Retinitis Pigmentosa 43 RTN133 RP43
Retinitis Pigmentosa 44 RTN136 RP44
Retinitis Pigmentosa 45 RTN159 RP45
Retinitis Pigmentosa 46 RTN130 RP46
Retinitis Pigmentosa 47 RTN143 RP47
Retinitis Pigmentosa 48 RTN147 RP48
Retinitis Pigmentosa 49 RTN129 RP49
Retinitis Pigmentosa 50 RTN210 RP50
Retinitis Pigmentosa 51 RTN106 RP51
Retinitis Pigmentosa 54 RTN085 RP54
Retinitis Pigmentosa 55 RTN090 RP55
Retinitis Pigmentosa 56 RTN116 RP56
Retinitis Pigmentosa 57 RTN117 RP57
Retinitis Pigmentosa 58 RTN114 RP58
Retinitis Pigmentosa 59 RTN171 RP59
Retinitis Pigmentosa 6 RTN068 RP6
Retinitis Pigmentosa 60 RTN160 RP60
Retinitis Pigmentosa 61 RTN144 RP61
Retinitis Pigmentosa 62 RTN146 RP62
Retinitis Pigmentosa 63 RTN148 RP63
Retinitis Pigmentosa 66 RTN152 RP66
Retinitis Pigmentosa 67 RTN140 RP67
Retinitis Pigmentosa 68 RTN165 RP68
Retinitis Pigmentosa 69 RTN166 RP69
Retinitis Pigmentosa 7 RTN069 RP7
Retinitis Pigmentosa 70 RTN169 RP70
Retinitis Pigmentosa 71 RTN176 RP71
Retinitis Pigmentosa 72 RTN178 RP72
Retinitis Pigmentosa 73 RTN177 RP73
Retinitis Pigmentosa 74 RTN180 RP74
Retinitis Pigmentosa 75 RTN186 RP75
Retinitis Pigmentosa 76 RTN190 RP76
Retinitis Pigmentosa 77 RTN192 RP77
Retinitis Pigmentosa 78 RTN196 RP78
Retinitis Pigmentosa 79 RTN195 RP79
Retinitis Pigmentosa 80 RTN213 RP80
Retinitis Pigmentosa 81 RTN214 RP81
Retinitis Pigmentosa 82 with or Without Situs Inversus RTN216 RPSI
Retinitis Pigmentosa 83 RTN217 RP83
Retinitis Pigmentosa 9 RTN070 RP9
Retinitis Pigmentosa and Erythrocytic Microcytosis RTN193 RPEM
Retinitis Pigmentosa Inversa with Deafness RTN205
Retinitis Pigmentosa with or Without Skeletal Anomalies RTN194 RPSKA
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 RPDSI
Retinitis Pigmentosa, Y-Linked RTN102 RPY
Retinitis Pigmentosa-Deafness Syndrome RTN187
Retinitis Pigmentosa-Intellectual Disability-Deafness-Hypogonadism Syndrome RTN215
Retinoblastoma RTN024 RB
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 XLRS1
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 RTT
Rett Syndrome, Congenital Variant RTT008 RTTCV
Reunion Island Larsen Syndrome RNN006 RLS
Reversible Cerebral Vasoconstriction Syndrome RVR002 RCVS
Revesz Syndrome RVS001 DKCA5
Reye Syndrome RYS001 RS
Reynolds Neri Hermann Syndrome RYN002
Reynolds Syndrome RYN003 REYNS
Rh Isoimmunization RHS001
Rhabditida Infections RHB006
Rhabdoid Cancer RHB001
Rhabdoid Meningioma RHB002
Rhabdoid Tumor Predisposition Syndrome 1 RHB008 RTPS1
Rhabdoid Tumor Predisposition Syndrome 2 RHB011 RTPS2
Rhabdomyomatous Mesenchymal Hamartoma RHB007 RMH
Rhabdomyosarcoma RHB003
Rhabdomyosarcoma 2 RHB024 RMS2
Rhabdomyosarcoma of the Cervix Uteri RHB019
Rhabdomyosarcoma of the Corpus Uteri RHB018
Rhabdomyosarcoma, Embryonal, 1 RHB023 RMSE1
Rhabdomyosarcoma, Embryonal, 2 RHB021 RMSE2
Rheumatic Disease RHM027
Rheumatic Encephalitis RHM016
Rheumatic Fever RHM001
Rheumatic Fever-Related Antigen RHM035
Rheumatic Heart Disease RHM028 RHD
Rheumatic Myocarditis RHM008
Rheumatic Pulmonary Valve Disease RHM002
Rheumatoid Arthritis RHM011 RA
Rheumatoid Arthritis, Systemic Juvenile RHM021 RASJ
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 RHINY
Rhizomelic Chondrodysplasia Punctata RHZ001 RCP
Rhizomelic Chondrodysplasia Punctata, Type 1 RHZ011 RCDP1
Rhizomelic Chondrodysplasia Punctata, Type 2 RHZ014 RCDP2
Rhizomelic Chondrodysplasia Punctata, Type 3 RHZ004 RCDP3
Rhizomelic Chondrodysplasia Punctata, Type 5 RHZ015 RCDP5
Rhizomelic Dysplasia, Patterson-Lowry Type RHZ012
Rhizomelic Dysplasia, Scoliosis, and Retinitis Pigmentosa RHZ006
Rhizomelic Pseudopolyarthritis RHZ007
Rhizomelic Syndrome RHZ008
Rh-Null, Amorph Type RHN014 RHNA
Rh-Null, Regulator Type RHN013 RHN
Rhombencephalosynapsis RHM015
Rhyns Syndrome RHY001
Ribbing Disease RBB001
Riboflavin Deficiency RBF001 RBFVD
Riboflavin Transporter Deficiency RBF003 BVVLS
Riboflavin Transporter Deficiency Neuronopathy RBF002 BVVLS
Ribose 5-Phosphate Isomerase Deficiency RBS005 RPID
Richards-Rundle Syndrome RCH002 RRS
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 VDDR
Rickettsia Parkeri Spotted Fever RCK001
Rickettsialpox RCK003
Riddle Syndrome RDD003 RIDDLES
Riedel's Fibrosing Thyroiditis RDL003
Rift Valley Fever RFT001
Right Aortic Arch RGH006
Right Atrial Isomerism RGH009 RAI
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 IRVH
Rigid Spine Muscular Dystrophy 1 RGD003 RSMD1
Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal RGD002 RMFSL
Ring Chromosome 1 RNG004 R1
Ring Chromosome 10 RNG005 R10
Ring Chromosome 11 RNG006 R11
Ring Chromosome 12 RNG007 R12
Ring Chromosome 13 RNG008 R13
Ring Chromosome 14 Syndrome RNG029
Ring Chromosome 15 RNG010 R15
Ring Chromosome 16 RNG011 R16
Ring Chromosome 17 RNG012 R17
Ring Chromosome 18 RNG013 R18
Ring Chromosome 19 RNG014 R19
Ring Chromosome 2 RNG015 R2
Ring Chromosome 20 RNG016 R20
Ring Chromosome 21 RNG017 R21
Ring Chromosome 22 RNG018 R22
Ring Chromosome 3 RNG019 R3
Ring Chromosome 4 RNG020 R4
Ring Chromosome 5 RNG021 R5
Ring Chromosome 6 RNG022 R6
Ring Chromosome 7 RNG023 R7
Ring Chromosome 8 RNG024 R8
Ring Chromosome 9 RNG025 R9
Ring Chromosome Y Syndrome RNG031 R
Ring Corneal Ulcer RNG002
Ring Dermoid of Cornea RNG003 RDC
Ring Staphyloma RNG001
Ringed Hair RNG030
Rippling Muscle Disease 1 RPP007 RMD1
Rippling Muscle Disease 2 RPP006 RMD2
Rippling Muscle Disease with Myasthenia Gravis RPP004
Ritscher-Schinzel Syndrome RTS001
Ritscher-Schinzel Syndrome 1 RTS003 RTSC1
Ritscher-Schinzel Syndrome 2 RTS002 RTSC2
Ritter's Disease RTT001 SSSS
Rnase T2-Deficient Leukoencephalopathy RNS005 CLWM
Roberts Syndrome RBR001 RBS
Robin Sequence with Cleft Mandible and Limb Anomalies RBN014 RCPS
Robin Sequence with Distinctive Facial Appearance and Brachydactyly RBN019
Robinow Syndrome RBN002
Robinow Syndrome, Autosomal Dominant 1 RBN018 DRS1
Robinow Syndrome, Autosomal Dominant 2 RBN017 DRS2
Robinow Syndrome, Autosomal Dominant 3 RBN020 DRS3
Robinow Syndrome, Autosomal Recessive RBN009 RRS
Robinow-Like Syndrome RBN010
Robinow-Sorauf Syndrome RBN013 RSS
Roch-Leri Mesosomatous Lipomatosis RCH009
Rocky Mountain Spotted Fever RCK002 RMSF
Rocuronium Allergy RCR031
Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction RDC015
Rodini Richieri Costa Syndrome RDN002
Rodrigues Blindness RDR002
Rohhad RHH001
Roifman Syndrome RFM001 RFMN
Roifman-Chitayat Syndrome RFM002
Rokitansky Sequence RKT002
Rokitansky-Aschoff Sinuses of the Gallbladder RKT003
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked RLN001 RESDX
Rolandic Epilepsy-Speech Dyspraxia Syndrome RLN004
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 RDD
Rosette-Forming Glioneuronal Tumor RST024 RGNT
Ross River Fever RSS001
Rosselli-Gulienetti Syndrome RSS006
Rothmund-Thomson Syndrome RTH001 RTS
Round Ligament Malignant Neoplasm RND001
Roussy-Levy Hereditary Areflexic Dystasia RSS026 ROULS
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 RSTS1
Rubinstein-Taybi Syndrome 2 RBN008 RSTS2
Rud Syndrome RDS004
Rudiger Syndrome RDG003
Ruijs-Aalfs Syndrome RJS001 RJALS
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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