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, 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 Disorder RDT017
Radiation-Induced Plexopathy RDT016
Radiculoneuropathy, Fatal Neonatal RDC014
Radiculopathy RDC002
Radin Blood Group Antigen RDN004 RD
Radio Renal Syndrome RDR001
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 Interstitial Lung Disease with Brain Calcifications RJB002 RILDBC
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 RHS
Rare Acquired Aplastic Anemia RRC002
Rare Acquired Deficiency Anemia RRC008
Rare Acquired Hemolytic Anemia RRC006
Rare Adenocarcinoma of the Breast RRD004
Rare Adrenal Disease RRD068
Rare Adult Hypothyroidism RRD014
Rare Allergic Respiratory Disease RRL004
Rare Arteriovenous Malformation RRR004
Rare Ataxia RRT024
Rare Atrial Defect and Interatrial Communication RRT022
Rare Autonomic Nervous System Disorder RRT016
Rare Bacterial Infectious Disease RRB003
Rare Benign Breast Tumor RRB002
Rare Benign Ovarian Tumor RRB001
Rare Biliary Tract Disease RRB009
Rare Bone Development Disorder RRB006
Rare Bone Disease Related to a Common Gene or Pathway Defect RRB007
Rare Brainstem or Cerebellar Disorder with Ophthalmic Involvement As a Major Feature RRB008
Rare Breast Malformation RRB005
Rare Breast Tumor RRB004
Rare Bronchopulmonary Tumor RRB010
Rare Cancer of Cervix Uteri RRC012
Rare Cancer of Corpus Uteri RRC011
Rare Capillary Malformation RRC010
Rare Capillary Malformation with Associated Anomalies RRC017
Rare Carcinoma of Pancreas RRC013
Rare Carcinoma of Small Intestine RRC019
Rare Carcinoma of Stomach RRC018
Rare Cardiac Rhythm Disease RRC014
Rare Cardiac Tumor RRC003
Rare Cardiomyopathy RRC004
Rare Cause of Hypertension RRC029
Rare Central Nervous System and Retinal Vascular Disease RRC021
Rare Cerebrovascular Dementia RRC034
Rare Choreic Movement Disorder RRC015
Rare Choroidal Disorder RRC025
Rare Chromosomal Anomaly RRC022
Rare Coagulation Disorder RRC033
Rare Combined Vascular Malformation RRC016
Rare Congenital Anomaly of Ventricular Septum RRC020
Rare Congenital Non-Syndromic Heart Malformation RRC028
Rare Conjunctivitis RRC026
Rare Constitutional Anemia RRC005
Rare Constitutional Aplastic Anemia RRC023
Rare Constitutional Hemolytic Anemia RRC007
Rare Constitutional Hemolytic Anemia Due to a Red Cell Membrane Anomaly RRC032
Rare Constitutional Hemolytic Anemia Due to an Enzyme Disorder RRC031
Rare Corneal Disorder RRC027
Rare Cutaneous Lichen Planus RRC009
Rare Cutaneous Lupus Erythematosus RRC001
Rare Deafness RRD005
Rare Deficiency Anemia RRD019
Rare Dementia RRD051
Rare Developmental Defect with Connective Tissue Involvement RRD017
Rare Developmental Defect with Skin/mucosae Involvement RRD016
Rare Diabetes Mellitus RRD067
Rare Diabetes Mellitus Type 1 RRD012
Rare Diabetes Mellitus Type 2 RRD013
Rare Digestive Tumor RRD054
Rare Disease in Anaesthesiology RRD057
Rare Disease in Plastic and Reconstructive Surgery RRD055
Rare Disease in Surgical Orthopedic RRD056
Rare Disease Involving Intestinal Motility RRD065
Rare Disease with Autism RRD010
Rare Disease with Cushing Syndrome As a Major Feature RRD020
Rare Disease with Dentinogenesis Imperfecta RRD009
Rare Disease with Disability RRD029
Rare Disease with Glaucoma As a Major Feature RRD063
Rare Disease with Malignant Hyperthermia RRD027
Rare Disease with Myoclonus As a Major Feature RRD026
Rare Disease with Odontological Manifestation RRD058
Rare Disease with Pierre Robin Syndrome RRD018
Rare Disease with Thoracic Aortic Aneurysm and Aortic Dissection RRD022
Rare Disorder Due to Poisoning RRD040
Rare Disorder Involving Multiple Structures of the Eye RRD041
Rare Disorder of the Anterior Segment of the Eye RRD049
Rare Disorder of the Lacrimal Apparatus RRD060
Rare Disorder of the Ocular Adnexa RRD047
Rare Disorder of the Posterior Segment of the Eye RRD044
Rare Disorder of the Pupil RRD050
Rare Disorder of the Visual Organs RRD052
Rare Disorder Potentially Indicated for Bowel Transplant RRD030
Rare Disorder Potentially Indicated for Heart Transplant RRD033
Rare Disorder Potentially Indicated for Hematopoietic Stem Cell Transplant RRD031
Rare Disorder Potentially Indicated for Kidney Transplant RRD035
Rare Disorder Potentially Indicated for Liver Transplant RRD034
Rare Disorder Potentially Indicated for Lung Transplant RRD032
Rare Disorder Related with Pregnancy, Childbirth and Puerperium RRD008
Rare Disorder with a Moyamoya Angiopathy RRD037
Rare Disorder with Conjunctival Involvement As a Major Feature RRD059
Rare Disorder with Corneal Involvement As a Major Feature RRD048
Rare Disorder with Dystonia and Other Neurologic or Systemic Manifestation RRD021
Rare Disorder with Ectropion RRD045
Rare Disorder with Entropion RRD046
Rare Disorder with Hirschsprung Disease As a Major Feature RRD038
Rare Disorder with Hypergonadotropic Hypogonadism RRD015
Rare Disorder with Hypertrichosis RRD053
Rare Disorder with Hypogonadotropic Hypogonadism RRD011
Rare Disorder with Lens Opacification RRD062
Rare Disorder with Obstructive Azoospermia RRD028
Rare Disorder with Optic Disc Malformation RRD042
Rare Disorder with Pigmented Sclera RRD043
Rare Disorder with Ptosis RRD061
Rare Disorder with Rch Resources Uncovered Otherwise RRD024
Rare Disorder with Strabismus RRD064
Rare Disorder Without Orphan Designation RRD023
Rare Dyslipidemia RRD066
Rare Dystonia RRD039
Rare Endocrine Growth Disease RRN018
Rare Epilepsy RRP028
Rare Epithelial Tumor of Colon RRP012
Rare Epithelial Tumor of Liver and Intrahepatic Biliary Tract RRP015
Rare Epithelial Tumor of Pancreas RRP011
Rare Epithelial Tumor of Rectum RRP013
Rare Epithelial Tumor of Small Intestine RRP014
Rare Epithelial Tumor of Stomach RRP018
Rare Eye Tumor RRY003
Rare Eyebrow/eyelash Disorder RRY001
Rare Eyelid Malposition Disorder RRY002
Rare Familial Disorder with Hypertrophic Cardiomyopathy RRF013
Rare Female Infertility RRF012
Rare Female Infertility Due to a Congenital Hypogonadotropic Hypogonadism RRF008
Rare Female Infertility Due to Adrenal Disorder of Genetic Origin RRF005
Rare Female Infertility Due to an Adrenal Disorder RRF011
Rare Female Infertility Due to an Anomaly of Ovarian Function RRF010
Rare Female Infertility Due to an Anomaly of Ovarian Function of Genetic Origin RRF004
Rare Female Infertility Due to an Implantation Defect RRF002
Rare Female Infertility Due to Gonadal Dysgenesis RRF003
Rare Female Infertility Due to Hypothalamic-Pituitary-Gonadal Axis Disorder RRF009
Rare Female Infertility Due to Hypothalamic-Pituitary-Gonadal Axis Disorder of Genetic Origin RRF006
Rare Female Infertility Due to Oocyte Maturation Defect RRF007
Rare Form of Salmonellosis RRF001
Rare Gastroesophageal Disease RRG075
Rare Gastroesophageal Tumor RRG003
Rare Genetic Adrenal Disease RRG009
Rare Genetic Autonomic Nervous System Disorder RRG039
Rare Genetic Bone Development Disorder RRG037
Rare Genetic Bone Disease RRG015
Rare Genetic Brainstem or Cerebellar Disorder with Ophthalmic Involvement As a Major Feature RRG070
Rare Genetic Capillary Malformation RRG031
Rare Genetic Cardiac Disease RRG072
Rare Genetic Choroidal Disorder RRG045
Rare Genetic Coagulation Disorder RRG008
Rare Genetic Conjunctivitis RRG055
Rare Genetic Corneal Disorder RRG054
Rare Genetic Developmental Defect During Embryogenesis RRG014
Rare Genetic Diabetes Mellitus RRG011
Rare Genetic Disease with Myoclonus As a Major Feature RRG028
Rare Genetic Disorder Involving Multiple Structures of the Eye RRG048
Rare Genetic Disorder of the Anterior Segment of the Eye RRG058
Rare Genetic Disorder of the Lacrimal Apparatus RRG060
Rare Genetic Disorder of the Ocular Adnexa RRG064
Rare Genetic Disorder of the Posterior Segment of the Eye RRG052
Rare Genetic Disorder of the Pupil RRG049
Rare Genetic Disorder of the Visual Organs RRG071
Rare Genetic Disorder with Conjunctival Involvement As a Major Feature RRG056
Rare Genetic Disorder with Corneal Involvement As a Major Feature RRG053
Rare Genetic Disorder with Entropion RRG059
Rare Genetic Disorder with Lens Opacification RRG057
Rare Genetic Disorder with Obstructive Azoospermia RRG035
Rare Genetic Disorder with Strabismus RRG065
Rare Genetic Dystonia RRG038
Rare Genetic Endocrine Disease RRG020
Rare Genetic Epilepsy RRG018
Rare Genetic Eye Disease RRG076
Rare Genetic Eyelid Malposition Disorder RRG062
Rare Genetic Female Infertility RRG034
Rare Genetic Gastroenterological Disease RRG002
Rare Genetic Gynecological and Obstetrical Diseases RRG007
Rare Genetic Headache RRG019
Rare Genetic Hematologic Disease RRG024
Rare Genetic Hepatic Disease RRG023
Rare Genetic Hyperkinetic Movement Disorder RRG040
Rare Genetic Hypothalamic or Pituitary Disease RRG010
Rare Genetic Immune Disease RRG005
Rare Genetic Inflammatory/autoimmune Corneal Disorder RRG050
Rare Genetic Intellectual Disability RRG006
Rare Genetic Macular Disorder RRG046
Rare Genetic Male Infertility RRG036
Rare Genetic Medullar Disease RRG017
Rare Genetic Movement Disorder RRG016
Rare Genetic Myoclonus RRG030
Rare Genetic Neurological Disorder RRG042
Rare Genetic Neuromuscular Disorder with Ocular Motility/alignment Anomaly RRG063
Rare Genetic Ocular Motility/alignment Disorder RRG066
Rare Genetic Odontal or Periodontal Disorder RRG001
Rare Genetic Odontologic Disease RRG041
Rare Genetic Ophthalmic Disorder with Cortical Involvement RRG069
Rare Genetic Ophthalmic Disorder with Cranial Nerve Involvement RRG067
Rare Genetic Optic Nerve Disorder RRG068
Rare Genetic Palpebral Disorder RRG061
Rare Genetic Parathyroid Disease and Phosphocalcic Metabolism Disorder RRG012
Rare Genetic Parkinsonian Disorder RRG027
Rare Genetic Renal Disease RRG073
Rare Genetic Respiratory Disease RRG022
Rare Genetic Retinal Disorder RRG051
Rare Genetic Retinal Vasculopathy RRG047
Rare Genetic Skin Disease RRG043
Rare Genetic Syndromic Intellectual Disability RRG004
Rare Genetic Systemic or Rheumatologic Disease RRG025
Rare Genetic Thyroid Disease RRG013
Rare Genetic Tremor Disorder RRG029
Rare Genetic Tumor RRG044
Rare Genetic Urogenital Disease RRG021
Rare Genetic Vascular Disease RRG026
Rare Genetic Vascular Tumor RRG032
Rare Genetic Venous Malformation RRG033
Rare Gynecological Tumor RRG074
Rare Head and Neck Malformation RRH012
Rare Head and Neck Tumor RRH024
Rare Headache RRH030
Rare Hemolytic Anemia RRH032
Rare Hemorrhagic Disorder RRH015
Rare Hemorrhagic Disorder Due to a Coagulation Factors Defect RRH014
Rare Hemorrhagic Disorder Due to a Constitutional Coagulation Factors Defect RRH029
Rare Hemorrhagic Disorder Due to a Constitutional Platelet Anomaly RRH028
Rare Hemorrhagic Disorder Due to a Constitutional Thrombocytopenia RRH017
Rare Hemorrhagic Disorder Due to a Platelet Anomaly RRH013
Rare Hemorrhagic Disorder Due to a Qualitative Platelet Defect RRH018
Rare Hemorrhagic Disorder Due to an Acquired Coagulation Factor Defect RRH002
Rare Hemorrhagic Disorder Due to an Acquired Platelet Anomaly RRH016
Rare Hepatic and Biliary Tract Tumor RRH033
Rare Hereditary Ataxia RRH004
Rare Hereditary Disease with Avascular Necrosis RRH025
Rare Hereditary Disease with Peripheral Neuropathy RRH001
Rare Hereditary Hemochromatosis RRH023
Rare Hereditary Metabolic Disease with Peripheral Neuropathy RRH020
Rare Hereditary Neurologic Disease with Peripheral Neuropathy RRH021
Rare Hereditary Systemic Disease with Peripheral Neuropathy RRH019
Rare Hereditary Thrombophilia RRH022
Rare Hypercholesterolemia RRH027
Rare Hyperkinetic Movement Disorder RRH026
Rare Hyperlipidemia RRH006
Rare Hyperopia and Astigmatism RRH031
Rare Hyperparathyroidism RRH011
Rare Hyperthyroidism RRH008
Rare Hypoaldosteronism RRH005
Rare Hypolipidemia RRH007
Rare Hypoparathyroidism RRH010
Rare Hypothalamic or Pituitary Disease RRH003
Rare Hypothyroidism RRH009
Rare Idiopathic Macular Telangiectasia RRD036
Rare Idiopathic Male Infertility RRD006
Rare Infertility RRN020
Rare Inflammatory Bowel Disease RRN022
Rare Inflammatory/autoimmune Corneal Disorder RRN016
Rare Insulin-Resistance Syndrome RRN005
Rare Intellectual Disability RRN017
Rare Intellectual Disability Without Developmental Anomaly RRN002
Rare Intestinal Disease RRN023
Rare Intoxication Due to Medical Products RRN014
Rare Isolated Myopia RRS002
Rare Lens Disease RRL005
Rare Lichen Planus RRL001
Rare Lymphatic Malformation RRL003 LM
Rare Lymphatic System Malformation RRL002
Rare Macular Disorder RRM014
Rare Male Infertility RRM015
Rare Male Infertility Due to Adrenal Disorder RRM012
Rare Male Infertility Due to Adrenal Disorder of Genetic Origin RRM009
Rare Male Infertility Due to Hypothalamic-Pituitary-Gonadal Axis Disorder RRM013
Rare Male Infertility Due to Hypothalamic-Pituitary-Gonadal Axis Disorder of Genetic Origin RRM010
Rare Male Infertility Due to Testicular Endocrine Disorder RRM011
Rare Malignant Breast Tumor RRM003
Rare Metabolic Liver Disease RRM017
Rare Movement Disorder RRM016
Rare Mucosal Lichen Planus RRM007
Rare Mycosis RRM006
Rare Myoclonus RRM008
Rare Nail Tumor RRN013
Rare Nervous System Tumor RRN019
Rare Neurodegenerative Disease RRN010
Rare Neuroinflammatory or Neuroimmunological Disease RRN009
Rare Neurologic Disease with Psychiatric Involvement RRN021
Rare Neuromuscular Disorder with Ocular Motility/alignment Anomaly RRN015
Rare Nevus RRN012
Rare Non Surgically Correctable Form of Primary Aldosteronism RRN011
Rare Non-Malformative Breast Disease RRN006
Rare Non-Malformative Gynecologic or Obstetric Disease RRN007
Rare Non-Malformative Uterine Adnexal Disease RRN004
Rare Non-Malformative Uterovaginal or Vulvovaginal Disease RRN008
Rare Ocular Motility/alignment Disorder RRC024
Rare Oculomotor Nerve Disorder RRC030
Rare Odontal or Periodontal Disorder RRD007
Rare Odontogenic Tumor RRD025
Rare Ophthalmic Disorder with Cortical Involvement RRP023
Rare Ophthalmic Disorder with Cranial Nerve Involvement RRP021
Rare Optic Nerve Disorder RRP022
Rare Otorhinolaryngologic Tumor RRT019
Rare Otorhinolaryngological Malformation RRT021
Rare Palpebral Disorder RRP026
Rare Pancreatic Disease RRP030
Rare Parasitic Disease RRP001
Rare Parathyroid Disease and Phosphocalcic Metabolism Anomaly RRP020
Rare Parathyroid Tumor RRP032
Rare Parenchymal Liver Disease RRP029
Rare Parkinsonian Disorder RRP019
Rare Parkinsonian Syndrome Due to Genetic Neurodegenerative Disease RRP008
Rare Parkinsonian Syndrome Due to Intoxication RRP009
Rare Parkinsonian Syndrome Due to Neurodegenerative Disease RRP010
Rare Paroxysmal Movement Disorder RRP007
Rare Pediatric Rheumatologic Disease RRP016
Rare Pediatric Systemic Disease RRP006
Rare Pediatric Vasculitis RRP005
Rare Peripheral Neuropathy RRP027
Rare Peripheral Precocious Puberty RRP003
Rare Pervasive Developmental Disorder RRP002
Rare Photodermatosis RRP024
Rare Precocious Puberty RRP025
Rare Primary Hyperaldosteronism RRP004
Rare Pulmonary Disease RRP031
Rare Pulmonary Hypertension RRP017
Rare Refraction Anomaly RRR012
Rare Renal Tubular Disease RRR011
Rare Renal Tumor RRR010
Rare Respiratory Tumor RRR009
Rare Retinal Disorder RRR006
Rare Retinal Vasculopathy RRR005
Rare Rheumatologic Disease RRR002
Rare Scleral Disorder RRS012
Rare Skin Tumor or Hamartoma RRS013
Rare Sleep Disorder RRS011
Rare Soft Tissue Tumor RRS010
Rare Sucking/swallowing Disorder RRS006
Rare Surgical Neurologic Disease RRS014
Rare Surgically Correctable Form of Primary Aldosteronism RRS009
Rare Syndrome with Cardiac Malformations RRS007
Rare Syndromic Dyslipidemia RRS005
Rare Syndromic Intellectual Disability RRS015
Rare Systemic Disease RRS004
Rare Systemic or Rheumatological Disease of Childhood RRS008
Rare Thrombotic Disease of Hematologic Origin RRT004
Rare Thrombotic Disorder Due to a Coagulation Factors Defect RRT010
Rare Thrombotic Disorder Due to a Constitutional Coagulation Factors Defect RRT009
Rare Thrombotic Disorder Due to a Constitutional Platelet Anomaly RRT006
Rare Thrombotic Disorder Due to a Platelet Anomaly RRT007
Rare Thrombotic Disorder Due to an Acquired Coagulation Factors Defect RRT008
Rare Thrombotic Disorder Due to an Acquired Platelet Anomaly RRT005
Rare Thyroid Disease RRT025
Rare Tremor Disorder RRT014
Rare Trochlear Nerve Disorder RRT018
Rare Tumor RRT020
Rare Tumor of Gallbladder and Extrahepatic Biliary Tract RRT015
Rare Tumor of Intestine RRT023
Rare Tumor of Neuroepithelial Tissue RRT011
Rare Tumor of Pancreas RRT002
Rare Tumor of Salivary Glands RRT012
Rare Tumor of Small Intestine RRT017
Rare Urinary Tract Tumor RRR008
Rare Urogenital Tumor RRR003
Rare Urticaria RRR007
Rare Uterine Adnexal Tumor RRT003
Rare Uterine Cancer RRT013
Rare Vaginal Malformation RRV004
Rare Variants of Adenocarcinoma of the Corpus Uteri RRV001
Rare Vascular Disease RRV009
Rare Vascular Liver Disease RRV010
Rare Vascular Malformation of Major Vessels RRV008
Rare Vascular Tumor RRV005
Rare Venous Malformation RRV006
Rare Viral Disease RRV002
Rare Virus Associated Tumor RRV007
Rare Vulvovaginal Tumor RRV003
Rasa1-Related Disorders RS1001
Ras-Associated Autoimmune Leukoproliferative Disorder RSS025 RALD
Rasmussen Encephalitis RSM001 RE
Rasmussen Johnsen Thomsen Syndrome RSM002
Rasmussen Subacute Encephalitis RSM003
Rasopathy RSP023
Rat Bite Fever RTB001
Ravine Syndrome RVN001
Raynaud Disease RYN001
Raynaud Phenomenon RYN005
Raynaud-Claes Syndrome RYN006 MRXSRC
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 RRQTL1
Rectal Cloacogenic Carcinoma RCT007
Rectal Disease RCT017
Rectal Duplication RCT033
Rectosigmoid Cancer RCT009
Rectosigmoid Junction Neoplasm RCT008
Rectum Adenocarcinoma RCT020
Rectum Adenoma RCT035
Rectum Cancer RCT021
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 Aplasia RDC006
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
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 Multilineage Dysplasia RFR009
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
Regional Odontodysplasia RGN005
Regional Ureteric Cancer RGN001
Regional Variant of Guillain-Barre Syndrome RGN006
Regular Astigmatism RGL001
Rela Fusion-Positive Ependymoma RLF001
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 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 Cell Carcinoma 4 RNL034 RCC4
Renal Cell Carcinoma, Nonpapillary RNL114 RCC
Renal Cell Carcinoma, Papillary, 1 RNL065 RCCP1
Renal Cell Carcinoma, Xp11-Associated RNL119 RCCX1
Renal Cysts and Diabetes Syndrome RNL051 RCAD
Renal Disease with Cataract RNL124
Renal Dysplasia RNL078
Renal Dysplasia Diffuse Cystic RNL036
Renal Dysplasia, Bilateral RNL107
Renal Dysplasia, Cystic RNL094 CYSRD
Renal Dysplasia, Unilateral RNL106
Renal Dysplasia-Limb Defects Syndrome RNL039 RL
Renal Failure, Progressive, with Hypertension RNL113 RFH1
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, Autosomal Dominant RNL046 AD-DRTA
Renal Tubular Acidosis, Distal, Autosomal Recessive RNL047 RTADR
Renal Tubular Acidosis, Distal, Type 3 RNL048
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 Wilms' Tumor RNL005
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
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
Rere-Related Disorders RRR001
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 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 Malformation RSP022
Respiratory or Mediastinal Malformation RSP024
Respiratory or Thoracic Malformation RSP025
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 Ciliopathy RTN220
Retinal Ciliopathy Due to Mutation in Bardet-Biedl Gene RTN222
Retinal Ciliopathy Due to Mutation in Nephronophthisis Gene RTN221
Retinal Ciliopathy Due to Mutation in the Retinitis Pigmentosa-1 Gene RTN223
Retinal Ciliopathy Due to Mutation in the Rpgr Gene RTN224
Retinal Ciliopathy Due to Mutation in the Rpgrip Gene RTN225
Retinal Ciliopathy Due to Mutation in Usher Gene RTN226
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
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 RP82
Retinitis Pigmentosa 83 RTN217 RP83
Retinitis Pigmentosa 84 RTN218 RP84
Retinitis Pigmentosa 85 RTN219 RP85
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 RB1
Retinochoroidal Coloboma RTN123
Retinohepatoendocrinologic Syndrome RTN072
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 RS1
Retinoschisis of Fovea RTN078
Retinoschisis, Autosomal Dominant RTN201
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-Like Syndrome RNN007
Reversible Cerebral Vasoconstriction Syndrome RVR002 RCVS
Revesz Syndrome RVS001 DKCA5
Reye Syndrome RYS001 RS
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 Interstitial Lung Disease RHM036
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 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 RHNR
Rhombencephalosynapsis RHM015
Rhyns Syndrome RHY001 RHYNS
Ribbing Disease RBB001
Riboflavin Deficiency RBF001 RBFVD
Riboflavin Transporter Deficiency RBF003 BVVLS
Riboflavin Transporter Deficiency Neuronopathy RBF002 BVVLS
Ribose 5-Phosphate Isomerase Deficiency RBS005 RPIAD
Richards-Rundle Syndrome RCH002 RRNS
Richieri Costa Da Silva Syndrome RCH003
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
Rickettsial Disease RCK009
Rickettsialpox RCK003
Riddle Syndrome RDD003 RIDL
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 RGD004 RSMD
Rigid Spine Muscular Dystrophy 1 RGD003 RSMD1
Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal RGD002 RMFSL
Ring Chromosome RNG032
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
Rnf13-Related Severe Early-Onset Epileptic Encephalopathy RNF001
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 1 RBN022 RRS1
Robinow Syndrome, Autosomal Recessive 2 RBN023 RRS2
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
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
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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