| OMIM ID |
Human Disease |
| 312190 |
Radial Aplasia, X-Linked |
| 179200 |
Radial Heads, Posterior Dislocation of |
| 179250 |
Radial Hypoplasia, Triphalangeal Thumbs, Hypospadias, and Maxillary Diastema |
| 312200 |
Radial Loop, Plain, on Right Index Finger |
| 300378 |
Radial Ray Deficiency, X-Linked |
| 179270 |
Radial Ray Hypoplasia with Choanal Atresia |
| 179280 |
Radial-Renal Syndrome |
| 605463 |
Radiation Sensitivity/Chromosome Instability Syndrome, Autosomal Dominant |
| 312210 |
Radiation Sensitivity of Natural Killer Activity |
| 266250 |
Radiculoneuropathy, Fatal Neonatal |
| 614416 |
Radiohumeral Fusions with Other Skeletal and Craniofacial Anomalies; |
| 179300 |
Radioulnar Synostosis |
| 300233 |
Radioulnar Synostosis, Radial Ray Abnormalities, and Severe Malformations in the Male |
| 266255 |
Radioulnar Synostosis, Unilateral, with Developmental Retardation and Hypotonia |
| 605432 |
Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia; RUSAT (1 mouse model) |
| 603438 |
Radioulnar Synostosis with Microcephaly, Short Stature, Scoliosis, and Mental Retardation |
| 179400 |
Radius, Aplasia of, with Cleft Lip/Palate |
| 179450 |
Ragweed Sensitivity |
| 179500 |
Raindrop Hypopigmentation |
| 259775 |
Raine Syndrome; RNS |
| 613658 |
Rajab Syndrome |
| 266270 |
Ramon Syndrome |
| 266280 |
Rapadilino Syndrome |
| 129400 |
Rapp-Hodgkin Syndrome; RHS |
| 179600 |
Raynaud Disease |
| 164761 |
Rearranged During Transfection Protooncogene; RET |
| 600878 |
Receptor Tyrosine Kinase Nsk2 |
| 179613 |
Recombinant Chromosome 8 Syndrome |
| 179650 |
Red Cell Permeability Defect |
| 179700 |
Red Cell Phospholipid Defect with Hemolysis |
| 266350 |
Red Skin Pigment Anomaly of New Guinea |
| 266400 |
Reese Retinal Dysplasia |
| 604335 |
Reflex Sympathetic Dystrophy |
| 266500 |
Refsum Disease, Classic (1 mouse model) |
| 602455 |
Regeneration-Associated Serpin-1 |
| 191830 |
Renal Adysplasia |
| 266810 |
Renal and Mullerian Duct Hypoplasia |
| 144700 |
Renal Cell Carcinoma, Nonpapillary; RCC |
| 605074 |
Renal Cell Carcinoma, Papillary, 1; RCCP1 |
| 300854 |
Renal Cell Carcinoma, Xp11-Associated; RCCX1 |
| 137920 |
Renal Cysts and Diabetes Syndrome |
| 601331 |
Renal Dysplasia, Cystic, Susceptibility To; CYSRD |
| 266910 |
Renal Dysplasia-Limb Defects Syndrome |
| 161900 |
Renal Failure, Progressive, with Hypertension; RFH1 |
| 267400 |
Renal, Genital, and Middle Ear Anomalies |
| 233100 |
Renal Glucosuria; GLYS1 |
| 208540 |
Renal-Hepatic-Pancreatic Dysplasia; RHPD |
| 610805 |
Renal Hypodysplasia, Nonsyndromic, 1; RHDNS1 |
| 179800 |
Renal Tubular Acidosis, Distal, Autosomal Dominant |
| 602722 |
Renal Tubular Acidosis, Distal, Autosomal Recessive; RTADR (2 mouse models) |
| 611590 |
Renal Tubular Acidosis, Distal, with Hemolytic Anemia |
| 611555 |
Renal Tubular Acidosis, Distal, with Nephrocalcinosis, Short Stature, Mental Retardation, and Distinctive Facies |
| 267300 |
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness |
| 267200 |
Renal Tubular Acidosis III |
| 179830 |
Renal Tubular Acidosis, Proximal (1 mouse model) |
| 604278 |
Renal Tubular Acidosis, Proximal, with Ocular Abnormalities and Mental Retardation |
| 267430 |
Renal Tubular Dysgenesis; RTD |
| 560000 |
Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia |
| 309500 |
Renpenning Syndrome 1; RENS1 |
| 267450 |
Respiratory Distress Syndrome in Premature Infants (4 mouse models) |
| 267480 |
Respiratory Underresponsiveness to Hypoxia and Hypercapnia |
| 607276 |
Resting Heart Rate, Variation in |
| 102300 |
Restless Legs Syndrome, Susceptibility to, 1; RLS1 |
| 608831 |
Restless Legs Syndrome, Susceptibility to, 2; RLS2 |
| 610438 |
Restless Legs Syndrome, Susceptibility to, 3; RLS3 |
| 610439 |
Restless Legs Syndrome, Susceptibility to, 4; RLS4 |
| 611242 |
Restless Legs Syndrome, Susceptibility to, 5; RLS5 |
| 611185 |
Restless Legs Syndrome, Susceptibility to, 6; RLS6 (1 mouse model) |
| 612853 |
Restless Legs Syndrome, Susceptibility to, 7 |
| 275210 |
Restrictive Dermopathy, Lethal (4 mouse models) |
| 267500 |
Reticular Dysgenesis |
| 179840 |
Reticular Dystrophy of Retinal Pigment Epithelium |
| 312500 |
Reticuloendotheliosis, X-Linked |
| 267730 |
Reticulum Cell Sarcoma |
| 179900 |
Retinal Aplasia |
| 614224 |
Retinal Arterial Macroaneurysm with Supravalvular Pulmonic Stenosis; |
| 180000 |
Retinal Arteries, Tortuosity of |
| 180020 |
Retinal Cone Dystrophy 1; RCD1 |
| 610024 |
Retinal Cone Dystrophy 3A; RCD3A |
| 610356 |
Retinal Cone Dystrophy 3b; RCD3B |
| 610478 |
Retinal Cone Dystrophy 4; RCD4 |
| 267740 |
Retinal Degeneration and Epilepsy |
| 267760 |
Retinal Degeneration with Nanophthalmos, Cystic Macular Degeneration, and Angle Closure Glaucoma |
| 312530 |
Retinal Detachment |
| 180050 |
Retinal Detachment |
| 312550 |
Retinal Dysplasia, Primary; PRD |
| 615147 |
Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome; RDCCAS |
| 267800 |
Retinal Dystrophy, Reticular Pigmentary, of Posterior Pole |
| 180070 |
Retinal Nonattachment and Falciform Detachment |
| 221900 |
Retinal Nonattachment, Nonsyndromic Congenital; RNANC |
| 267900 |
Retinal Telangiectasia and Hypogammaglobulinemia |
| 180080 |
Retinal Venous Beading |
| 180105 |
Retinitis Pigmentosa 10; RP10 |
| 600138 |
Retinitis Pigmentosa 11; RP11 (1 mouse model) |
| 600105 |
Retinitis Pigmentosa 12; RP12 (1 mouse model) |
| 600059 |
Retinitis Pigmentosa 13; RP13 (2 mouse models) |
| 600132 |
Retinitis Pigmentosa 14; RP14 (1 mouse model) |
| 600852 |
Retinitis Pigmentosa 17; RP17 |
| 601414 |
Retinitis Pigmentosa 18; RP18 (2 mouse models) |
| 601718 |
Retinitis Pigmentosa 19; RP19 (2 mouse models) |
| 180100 |
Retinitis Pigmentosa 1; RP1 (1 mouse model) |
| 613794 |
Retinitis Pigmentosa 20; RP20 (1 mouse model) |
| 602594 |
Retinitis Pigmentosa 22; RP22 |
| 300424 |
Retinitis Pigmentosa 23; RP23 |
| 300155 |
Retinitis Pigmentosa 24; RP24 |
| 602772 |
Retinitis Pigmentosa 25; RP25 |
| 608380 |
Retinitis Pigmentosa 26; RP26 |
| 613750 |
Retinitis Pigmentosa 27; RP27 |
| 606068 |
Retinitis Pigmentosa 28; RP28 |
| 612165 |
Retinitis Pigmentosa 29; RP29 |
| 312600 |
Retinitis Pigmentosa 2; RP2 |
| 607921 |
Retinitis Pigmentosa 30; RP30 (2 mouse models) |
| 609923 |
Retinitis Pigmentosa 31; RP31 |
| 609913 |
Retinitis Pigmentosa 32; RP32 |
| 610359 |
Retinitis Pigmentosa 33; RP33 |
| 300605 |
Retinitis Pigmentosa 34; RP34 |
| 610282 |
Retinitis Pigmentosa 35; RP35 |
| 610599 |
Retinitis Pigmentosa 36; RP36 |
| 611131 |
Retinitis Pigmentosa 37; RP37 |
| 613862 |
Retinitis Pigmentosa 38; RP38 |
| 613809 |
Retinitis Pigmentosa 39; RP39 |
| 300029 |
Retinitis Pigmentosa 3; RP3 (3 mouse models) |
| 613801 |
Retinitis Pigmentosa 40; RP40 |
| 612095 |
Retinitis Pigmentosa 41; RP41 (1 mouse model) |
| 612943 |
Retinitis Pigmentosa 42; RP42 |
| 613810 |
Retinitis Pigmentosa 43; RP43 |
| 613769 |
Retinitis Pigmentosa 44; RP44 |
| 613767 |
Retinitis Pigmentosa 45; RP45 |
| 612572 |
Retinitis Pigmentosa 46; RP46 |
| 613758 |
Retinitis Pigmentosa 47; RP47 |
| 613827 |
Retinitis Pigmentosa 48; RP48 |
| 613756 |
Retinitis Pigmentosa 49; RP49 |
| 613731 |
Retinitis Pigmentosa 4; RP4 (1 mouse model) |
| 613194 |
Retinitis Pigmentosa 50; RP50 |
| 613464 |
Retinitis Pigmentosa 51; RP51 |
| 613428 |
Retinitis Pigmentosa 54; RP54 |
| 613575 |
Retinitis Pigmentosa 55; RP55 |
| 613581 |
Retinitis Pigmentosa 56; RP56 |
| 613582 |
Retinitis Pigmentosa 57; RP57 |
| 613617 |
Retinitis Pigmentosa 58; RP58 |
| 613861 |
Retinitis Pigmentosa 59; RP59 |
| 613983 |
Retinitis Pigmentosa 60; RP60 |
| 614180 |
Retinitis Pigmentosa 61; RP61 |
| 614181 |
Retinitis Pigmentosa 62; RP62 |
| 614494 |
Retinitis Pigmentosa 63; RP63 |
| 312612 |
Retinitis Pigmentosa 6; RP6 |
| 608133 |
Retinitis Pigmentosa 7; RP7 (3 mouse models) |
| 180104 |
Retinitis Pigmentosa 9; RP9 |
| 268020 |
Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism |
| 500004 |
Retinitis Pigmentosa-Deafness Syndrome |
| 268010 |
Retinitis Pigmentosa Inversa with Deafness |
| 268025 |
Retinitis Pigmentosa, Late-Adult Onset |
| 268000 |
Retinitis Pigmentosa; RP (24 mouse models) |
| 300455 |
Retinitis Pigmentosa, X-Linked, and Sinorespiratory Infections, with or without Deafness |
| 400004 |
Retinitis Pigmentosa, Y-Linked; RPY |
| 180200 |
Retinoblastoma; RB1 (5 mouse models) |
| 268040 |
Retinohepatoendocrinologic Syndrome |
| 268060 |
Retinopathy, Pericentral Pigmentary, Autosomal Recessive |
| 180210 |
Retinopathy, Pericentral Pigmentary, Dominant |
| 268050 |
Retinopathy, Pigmentary, and Mental Retardation |
| 312700 |
Retinoschisis 1, X-Linked, Juvenile; RS1 (4 mouse models) |
| 180270 |
Retinoschisis, Autosomal Dominant |
| 268080 |
Retinoschisis of Fovea |
| 613454 |
Rett Syndrome, Congenital Variant |
| 312750 |
Rett Syndrome; RTT (18 mouse models) |
| 268130 |
Revesz Syndrome |
| 613471 |
Reynolds Syndrome |
| 609322 |
Rhabdoid Tumor Predisposition Syndrome 1; RTPS1 (1 mouse model) |
| 613325 |
Rhabdoid Tumor Predisposition Syndrome 2; RTPS2 |
| 268210 |
Rhabdomyosarcoma 1; RMS1 (1 mouse model) |
| 268220 |
Rhabdomyosarcoma 2; RMS2 (4 mouse models) |
| 268240 |
Rheumatic Fever-Related Antigen |
| 180300 |
Rheumatoid Arthritis; RA (14 mouse models) |
| 604302 |
Rheumatoid Arthritis, Systemic Juvenile |
| 180350 |
Rheumatoid Nodulosis |
| 180360 |
Rhiny |
| 215100 |
Rhizomelic Chondrodysplasia Punctata, Type 1; RCDP1 (2 mouse models) |
| 222765 |
Rhizomelic Chondrodysplasia Punctata, Type 2; RCDP2 (1 mouse model) |
| 600121 |
Rhizomelic Chondrodysplasia Punctata, Type 3; RCDP3 (1 mouse model) |
| 601438 |
Rhizomelic Dysplasia, Patterson-Lowry Type |
| 610319 |
Rhizomelic Dysplasia, Scoliosis, and Retinitis Pigmentosa |
| 268250 |
Rhizomelic Syndrome |
| 268150 |
Rh-Null, Regulator Type; RHN |
| 610576 |
Rho Gtpase-Activating Protein 9; ARHGAP9 |
| 602152 |
Rhyns Syndrome |
| 601477 |
Ribbing Disease |
| 615026 |
Riboflavin Deficiency; RBFVD |
| 608611 |
Ribose 5-Phosphate Isomerase Deficiency |
| 268850 |
Richieri-Costa/Guion-Almeida Syndrome |
| 611943 |
Riddle Syndrome |
| 610338 |
Right Pulmonary Artery, Anomalous Origin of, Familial |
| 277200 |
Right Ventricular Hypoplasia, Isolated |
| 614498 |
Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal; RMFSL |
| 602771 |
Rigid Spine Muscular Dystrophy 1; RSMD1 (1 mouse model) |
| 180550 |
Ring Dermoid of Cornea; RDC |
| 180600 |
Ringed Hair |
| 600332 |
Rippling Muscle Disease 1; RMD1 |
| 606072 |
Rippling Muscle Disease; RMD |
| 268300 |
Roberts Syndrome; RBS |
| 180750 |
Robinow-Sorauf Syndrome |
| 180700 |
Robinow Syndrome, Autosomal Dominant; DRS |
| 268310 |
Robinow Syndrome, Autosomal Recessive; RRS (2 mouse models) |
| 268305 |
Robin Sequence with Cleft Mandible and Limb Anomalies |
| 608670 |
Robin Sequence with Distinctive Facial Appearance and Brachydactyly |
| 268315 |
Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction |
| 268320 |
Rodrigues Blindness |
| 613328 |
Roifman-Chitayat Syndrome |
| 300258 |
Roifman Syndrome |
| 601085 |
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, Autosomal Dominant; RESDAD |
| 300643 |
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked; |
| 180730 |
Rombo Syndrome |
| 225000 |
Rosselli-Gulienetti Syndrome |
| 268400 |
Rothmund-Thomson Syndrome; RTS (3 mouse models) |
| 180800 |
Roussy-Levy Hereditary Areflexic Dystasia |
| 268500 |
Rowley-Rosenberg Syndrome |
| 180849 |
Rubinstein-Taybi Syndrome 1; RSTS1 (4 mouse models) |
| 613684 |
Rubinstein-Taybi Syndrome 2; RSTS2 |
| 268650 |
Rudiger Syndrome |
| 312780 |
Russell-Silver Syndrome, X-Linked |
| 180900 |
Rutherfurd Syndrome |
| 180870 |
Ruvalcaba Syndrome |
Analysis Tools