| OMIM ID |
Human Disease |
| 211390 |
Sabinas Brittle Hair Syndrome |
| 268700 |
Saccharopinuria |
| 600145 |
Sacral Defect with Anterior Meningocele (1 mouse model) |
| 101400 |
Saethre-Chotzen Syndrome; SCS (8 mouse models) |
| 610871 |
Sakoda Complex |
| 181010 |
Salivary Duct Calculi |
| 181030 |
Salivary Gland Adenoma, Pleomorphic |
| 180950 |
Salivary Substance, Clostridium Botulinum Type |
| 268800 |
Sandhoff Disease (8 mouse models) |
| 613005 |
Santos Syndrome |
| 609464 |
Sarcoidosis, Early-Onset |
| 181000 |
Sarcoidosis, Susceptibility to, 1; SS1 |
| 612387 |
Sarcoidosis, Susceptibility to, 2; SS2 |
| 612388 |
Sarcoidosis, Susceptibility to, 3; SS3 |
| 300813 |
Sarcoma, Synovial (3 mouse models) |
| 268900 |
Sarcosinemia; SARCOS |
| 600705 |
Satoyoshi Syndrome |
| 181180 |
Say Syndrome |
| 181200 |
SC(1) Trait of Saliva |
| 181250 |
Scalp Defects and Postaxial Polydactyly |
| 181270 |
Scalp-Ear-Nipple Syndrome |
| 609579 |
Scaphocephaly, Maxillary Retrusion, and Mental Retardation |
| 181300 |
Scapula, Contour of Vertebral Border of |
| 181430 |
Scapuloperoneal Myopathy, Myh7-Related; SPMM |
| 300695 |
Scapuloperoneal Myopathy, X-Linked Dominant; SPM |
| 181405 |
Scapuloperoneal Spinal Muscular Atrophy; SPSMA |
| 181400 |
Scapuloperoneal Syndrome, Neurogenic, Kaeser Type; SCPNK |
| 312830 |
SCARF Syndrome |
| 607016 |
Scheie Syndrome (1 mouse model) |
| 181440 |
Scheuermann Disease (2 mouse models) |
| 164220 |
Schilbach-Rott Syndrome |
| 312840 |
Schimke X-Linked Mental Retardation Syndrome |
| 163200 |
Schimmelpenning-Feuerstein-Mims Syndrome; SFM |
| 609241 |
Schindler Disease, Type I |
| 269150 |
Schinzel-Giedion Midface Retraction Syndrome |
| 181460 |
Schistosoma Mansoni Infection, Susceptibility/Resistance to |
| 269160 |
Schizencephaly |
| 605419 |
Schizophrenia 10; SCZD10 |
| 608078 |
Schizophrenia 11 |
| 608543 |
Schizophrenia 12 |
| 613025 |
Schizophrenia 13; SCZD13 |
| 612361 |
Schizophrenia 14 |
| 613950 |
Schizophrenia 15; SCZD15 |
| 613959 |
Schizophrenia 16; SCZD16 |
| 614332 |
Schizophrenia 17; SCZD17 |
| 181510 |
Schizophrenia 1; SCZD1 |
| 603342 |
Schizophrenia 2; SCZD2 |
| 600511 |
Schizophrenia 3; SCZD3 |
| 600850 |
Schizophrenia 4; SCZD4 |
| 603175 |
Schizophrenia 5; SCZD5 |
| 603013 |
Schizophrenia 6; SCZD6 |
| 603176 |
Schizophrenia 7; SCZD7 |
| 603206 |
Schizophrenia 8; SCZD8 |
| 604906 |
Schizophrenia 9; SCZD9 |
| 181500 |
Schizophrenia; SCZD (32 mouse models) |
| 269250 |
Schneckenbecken Dysplasia (1 mouse model) |
| 121800 |
Schnyder Corneal Dystrophy; SCCD |
| 181515 |
Scholte Syndrome |
| 224750 |
Schopf-Schulz-Passarge Syndrome; SSPS |
| 162091 |
Schwannomatosis |
| 255800 |
Schwartz-Jampel Syndrome, Type 1; SJS1 (4 mouse models) |
| 269300 |
Schwartz-Lelek Syndrome |
| 608281 |
Scimitar Anomaly, Multiple Cardiac Malformations, and Craniofacial and Central Nervous System Abnormalities |
| 181700 |
Sclerocornea, Autosomal Dominant |
| 269400 |
Sclerocornea, Autosomal Recessive |
| 181750 |
Scleroderma, Familial Progressive (4 mouse models) |
| 269500 |
Sclerosteosis 1; SOST1 |
| 614305 |
Sclerosteosis 2; SOST2 |
| 181600 |
Sclerotylosis |
| 612445 |
Scoliosis, Arachnodactyly, and Blindness |
| 181800 |
Scoliosis, Idiopathic, Susceptibility to, 1; IS1 |
| 607354 |
Scoliosis, Idiopathic, Susceptibility to, 2; IS2 |
| 608765 |
Scoliosis, Idiopathic, Susceptibility to, 3; IS3 |
| 612238 |
Scoliosis, Idiopathic, Susceptibility to, 4; IS4 |
| 612239 |
Scoliosis, Idiopathic, Susceptibility to, 5; IS5 |
| 312860 |
Scott Craniodigital Syndrome with Mental Retardation |
| 262890 |
Scott Syndrome; SCTS |
| 269000 |
SC Phocomelia Syndrome |
| 269600 |
Sea-Blue Histiocyte Disease |
| 601700 |
Sebaceous Gland Hyperplasia, Familial Presenile |
| 605249 |
Sebastian Syndrome; SBS |
| 610227 |
Seborrhea-Like Dermatitis with Psoriasiform Elements |
| 210600 |
Seckel Syndrome 1; SCKL1 (1 mouse model) |
| 606744 |
Seckel Syndrome 2; SCKL2 |
| 608664 |
Seckel Syndrome 3; SCKL3 |
| 613676 |
Seckel Syndrome 4; SCKL4 |
| 613823 |
Seckel Syndrome 5; SCKL5 |
| 614728 |
Seckel Syndrome 6; SCKL6 |
| 614851 |
Seckel Syndrome 7; SCKL7 |
| 269630 |
Second Metatarsal-Metacarpal Syndrome |
| 269650 |
Secretory Component Deficiency |
| 607540 |
Secretory Diarrhea, Myopathy, and Deafness |
| 605407 |
Segawa Syndrome, Autosomal Recessive |
| 601764 |
Seizures, Benign Familial Infantile, 1; BFIS1 |
| 605751 |
Seizures, Benign Familial Infantile, 2; BFIS2 |
| 607745 |
Seizures, Benign Familial Infantile, 3; BFIS3 |
| 612627 |
Seizures, Benign Familial Infantile, 4; BFIS4 |
| 121200 |
Seizures, Benign Familial Neonatal, 1; BFNS1 (5 mouse models) |
| 121201 |
Seizures, Benign Familial Neonatal, 2; BFNS2 (5 mouse models) |
| 608217 |
Seizures, Benign Familial Neonatal, 3; BFNS3 |
| 269720 |
Seizures, Benign Familial Neonatal, Autosomal Recessive |
| 612780 |
Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance; SESAMES |
| 173610 |
Selectin P; SELP |
| 269840 |
Selective T-Cell Defect; STCD |
| 182200 |
Sella Turcica, Bridged |
| 606156 |
Sener Syndrome |
| 212350 |
Sengers Syndrome |
| 269800 |
Senile Plaque Formation |
| 266900 |
Senior-Loken Syndrome 1; SLSN1 |
| 606995 |
Senior-Loken Syndrome 3; SLSN3 |
| 606996 |
Senior-Loken Syndrome 4; SLSN4 |
| 609254 |
Senior-Loken Syndrome 5; SLSN5 |
| 610189 |
Senior-Loken Syndrome 6; SLSN6 |
| 613615 |
Senior-Loken Syndrome 7; SLSN7 |
| 602340 |
Sensorineural Hearing Loss, Retinal Pigment Epithelium Lesions, Discolored Teeth |
| 607459 |
Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis; SANDO |
| 182230 |
Septooptic Dysplasia (3 mouse models) |
| 600598 |
Setting-Sun Phenomenon, Familial Benign |
| 102700 |
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency (1 mouse model) |
| 601457 |
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Positive (2 mouse models) |
| 600802 |
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Negative |
| 608971 |
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Positive (6 mouse models) |
| 611291 |
Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation |
| 602450 |
Severe Combined Immunodeficiency with Sensitivity to Ionizing Radiation (2 mouse models) |
| 300400 |
Severe Combined Immunodeficiency, X-Linked; SCIDX1 |
| 608579 |
Severe Cutaneous Adverse Reaction, Susceptibility to |
| 613498 |
Sex Hormone-Binding Globulin Circulating Level Quantitative Trait Locus; SXGQTL1 |
| 200900 |
Short-Limb Skeletal Dysplasia with Severe Combined Immunodeficiency |
| 609620 |
Short Qt Syndrome 1; SQT1 (1 mouse model) |
| 609621 |
Short Qt Syndrome 2; SQT2 |
| 609622 |
Short Qt Syndrome 3; SQT3 |
| 263520 |
Short Rib-Polydactyly Syndrome, Type IIA |
| 615087 |
Short Rib-Polydactyly Syndrome, Type IIB |
| 263510 |
Short Rib-Polydactyly Syndrome, Type III (2 mouse models) |
| 263530 |
Short Rib-Polydactyly Syndrome, Type I; SRPS1 |
| 269860 |
Short Rib-Polydactyly Syndrome, Type IV |
| 614091 |
Short Rib-Polydactyly Syndrome, Type V; SRPS5 |
| 609654 |
Short Stature and Facioauriculothoracic Malformations |
| 602471 |
Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, Skeletal Abnormalities |
| 604271 |
Short Stature, Idiopathic, Autosomal |
| 300582 |
Short Stature, Idiopathic, X-Linked; ISS |
| 605856 |
Short Stature, Mental Retardation, Callosal Agenesis, Heminasal Hypoplasia, Microphthalmia, and Atypical Clefting |
| 269870 |
Short Stature-Obesity Syndrome; SSOS |
| 614813 |
Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis; |
| 614800 |
Short Stature, Optic Nerve Atrophy, and Pelger-Huet Anomaly; SOPH |
| 601350 |
Short Stature Syndrome, Brussels Type |
| 269880 |
SHORT Syndrome |
| 600269 |
Short Tarsus with Absence of Lower Eyelashes; STALE |
| 182212 |
Shprintzen-Goldberg Craniosynostosis Syndrome; SGS |
| 182210 |
Shprintzen Omphalocele Syndrome |
| 260400 |
Shwachman-Diamond Syndrome; SDS (3 mouse models) |
| 269921 |
Sialuria |
| 604369 |
Sialuria, Finnish Type (1 mouse model) |
| 603903 |
Sickle Cell Anemia (5 mouse models) |
| 608567 |
Sick Sinus Syndrome 1, Autosomal Recessive; SSS1 |
| 163800 |
Sick Sinus Syndrome 2, Autosomal Dominant; SSS2 |
| 614090 |
Sick Sinus Syndrome 3, Susceptibility To; SSS3 |
| 300263 |
Siderius X-Linked Mental Retardation Syndrome; MRXSSD |
| 180860 |
Silver-Russell Syndrome; SRS |
| 182150 |
Simosa Craniofacial Syndrome |
| 312870 |
Simpson-Golabi-Behmel Syndrome, Type 1; SGBS1 (8 mouse models) |
| 300209 |
Simpson-Golabi-Behmel Syndrome, Type 2 |
| 182250 |
Singleton-Merten Syndrome (1 mouse model) |
| 614896 |
Sinoatrial Node Dysfunction and Deafness; SANDD |
| 182190 |
Sinus Node Disease and Myopia |
| 182220 |
Sister Chromatid Exchange, Frequency of |
| 210250 |
Sitosterolemia (3 mouse models) |
| 603643 |
Situs Inversus Totalis with Cystic Dysplasia of Kidneys and Pancreas |
| 270220 |
Sjogren-Larsson-Like Ichthyosis without Cns or Eye Involvement |
| 270200 |
Sjogren-Larsson Syndrome; SLS |
| 270150 |
Sjogren Syndrome (22 mouse models) |
| 612447 |
Skeletal Defects, Genital Hypoplasia, and Mental Retardation |
| 602613 |
Skeletal Dysplasia and Progressive Central Nervous System Degeneration, Lethal |
| 609047 |
Skeletal Dysplasia, Rhizomelic, with Retinitis Pigmentosa |
| 182255 |
Skeletal Dysplasia with Delayed Epiphyseal and Carpal Bone Ossification |
| 156610 |
Skin Creases, Multiple Benign Ring-Shaped, of Limbs |
| 607655 |
Skin Fragility-Woolly Hair Syndrome; SFWHS |
| 612267 |
Skin/Hair/Eye Pigmentation, Variation In, 10; SHEP10 |
| 612271 |
Skin/Hair/Eye Pigmentation, Variation In, 11; SHEP11 |
| 611664 |
Skin/Hair/Eye Pigmentation, Variation In, 7; SHEP7 |
| 611724 |
Skin/Hair/Eye Pigmentation, Variation In, 8; SHEP8 |
| 611742 |
Skin/Hair/Eye Pigmentation, Variation In, 9; SHEP9 |
| 270350 |
Skunk N-Butylmercaptan, Inability to Smell |
| 182260 |
Slipped Femoral Capital Epiphyses |
| 608236 |
Slowed Nerve Conduction Velocity, Autosomal Dominant |
| 182280 |
Small Cell Cancer of the Lung (4 mouse models) |
| 147891 |
Small Patella Syndrome; SPS |
| 270400 |
Smith-Lemli-Opitz Syndrome; SLOS (4 mouse models) |
| 182290 |
Smith-Magenis Syndrome; SMS (4 mouse models) |
| 607326 |
Smith-Mccort Dysplasia; SMC (1 mouse model) |
| 612052 |
Smoking As A Quantitative Trait Locus 3; SQTL3 |
| 182410 |
Sneddon Syndrome |
| 270425 |
Sodium-Potassium-Atpase Activity of Red Cell |
| 613508 |
Sodium Serum Level Quantitative Trait Locus 1; SSQTL1 |
| 147250 |
Solitary Median Maxillary Central Incisor; SMMCI |
| 614689 |
Soluble Interleukin-6 Receptor, Serum Level of, Quantitative Trait Locus |
| 109270 |
Solute Carrier Family 4 (anion Exchanger), Member 1; SLC4A1 (1 mouse model) |
| 182400 |
Somatomedin, Embryonic |
| 270460 |
Sonoda Syndrome |
| 117550 |
Sotos Syndrome 1; SOTOS1 (1 mouse model) |
| 614753 |
Sotos Syndrome 2; SOTOS2 |
| 108600 |
Spastic Ataxia 1, Autosomal Dominant; SPAX1 |
| 611302 |
Spastic Ataxia 2, Autosomal Recessive; SPAX2 |
| 611390 |
Spastic Ataxia 3, Autosomal Recessive; SPAX3 |
| 613672 |
Spastic Ataxia 4, Autosomal Recessive; SPAX4 |
| 614487 |
Spastic Ataxia 5, Autosomal Recessive; SPAX5 |
| 108650 |
Spastic Ataxia 7, Autosomal Dominant; SPAX7 |
| 270550 |
Spastic Ataxia, Charlevoix-Saguenay Type; SACS |
| 270600 |
Spastic Diplegia, Infantile Type (1 mouse model) |
| 607225 |
Spastic Paralysis, Infantile-Onset Ascending; IAHSP |
| 312910 |
Spastic Paraparesis and Deafness |
| 604187 |
Spastic Paraplegia 10, Autosomal Dominant; SPG10 |
| 604360 |
Spastic Paraplegia 11, Autosomal Recessive; SPG11 |
| 604805 |
Spastic Paraplegia 12, Autosomal Dominant; SPG12 |
| 605280 |
Spastic Paraplegia 13, Autosomal Dominant; SPG13 |
| 605229 |
Spastic Paraplegia 14, Autosomal Recessive; SPG14 |
| 270700 |
Spastic Paraplegia 15, Autosomal Recessive; SPG15 |
| 300266 |
Spastic Paraplegia 16, X-Linked; SPG16 |
| 270685 |
Spastic Paraplegia 17, Autosomal Dominant; SPG17 |
| 611225 |
Spastic Paraplegia 18, Autosomal Recessive; SPG18 |
| 607152 |
Spastic Paraplegia 19, Autosomal Dominant; SPG19 |
| 275900 |
Spastic Paraplegia 20, Autosomal Recessive; SPG20 (1 mouse model) |
| 270750 |
Spastic Paraplegia 23; SPG23 |
| 607584 |
Spastic Paraplegia 24, Autosomal Recessive; SPG24 |
| 608220 |
Spastic Paraplegia 25, Autosomal Recessive; SPG25 |
| 609195 |
Spastic Paraplegia 26, Autosomal Recessive; SPG26 |
| 609041 |
Spastic Paraplegia 27, Autosomal Recessive; SPG27 |
| 609340 |
Spastic Paraplegia 28, Autosomal Recessive; SPG28 |
| 609727 |
Spastic Paraplegia 29, Autosomal Dominant; SPG29 |
| 312920 |
Spastic Paraplegia 2, X-Linked; SPG2 (1 mouse model) |
| 610357 |
Spastic Paraplegia 30, Autosomal Recessive; SPG30 |
| 610250 |
Spastic Paraplegia 31, Autosomal Dominant; SPG31 |
| 611252 |
Spastic Paraplegia 32, Autosomal Recessive; SPG32 |
| 610244 |
Spastic Paraplegia 33, Autosomal Dominant; SPG33 |
| 300750 |
Spastic Paraplegia 34, X-Linked; SPG34 |
| 612319 |
Spastic Paraplegia 35, Autosomal Recessive; SPG35 (1 mouse model) |
| 613096 |
Spastic Paraplegia 36, Autosomal Dominant; SPG36 |
| 611945 |
Spastic Paraplegia 37, Autosomal Dominant; SPG37 |
| 612335 |
Spastic Paraplegia 38, Autosomal Dominant; SPG38 |
| 612020 |
Spastic Paraplegia 39, Autosomal Recessive; SPG39 |
| 182600 |
Spastic Paraplegia 3, Autosomal Dominant; SPG3A |
| 613364 |
Spastic Paraplegia 41, Autosomal Dominant; SPG41 |
| 612539 |
Spastic Paraplegia 42, Autosomal Dominant; SPG42 |
| 615043 |
Spastic Paraplegia 43, Autosomal Recessive; SPG43 |
| 613206 |
Spastic Paraplegia 44, Autosomal Recessive; SPG44 |
| 613162 |
Spastic Paraplegia 45, Autosomal Recessive; SPG45 |
| 614409 |
Spastic Paraplegia 46, Autosomal Recessive; SPG46 |
| 614066 |
Spastic Paraplegia 47, Autosomal Recessive; SPG47 |
| 613647 |
Spastic Paraplegia 48, Autosomal Recessive; SPG48 |
| 615031 |
Spastic Paraplegia 49, Autosomal Recessive; SPG49 |
| 182601 |
Spastic Paraplegia 4, Autosomal Dominant; SPG4 (2 mouse models) |
| 612936 |
Spastic Paraplegia 50, Autosomal Recessive; SPG50 |
| 613744 |
Spastic Paraplegia 51, Autosomal Recessive; SPG51 |
| 614067 |
Spastic Paraplegia 52, Autosomal Recessive; SPG52 |
| 614898 |
Spastic Paraplegia 53, Autosomal Recessive; SPG53 |
| 615033 |
Spastic Paraplegia 54, Autosomal Recessive; SPG54 |
| 615035 |
Spastic Paraplegia 55, Autosomal Recessive; SPG55 |
| 615030 |
Spastic Paraplegia 56, Autosomal Recessive; SPG56 |
| 270800 |
Spastic Paraplegia 5A, Autosomal Recessive; SPG5A |
| 600146 |
Spastic Paraplegia 5B, Autosomal Recessive; SPG5B |
| 600363 |
Spastic Paraplegia 6, Autosomal Dominant; SPG6 |
| 607259 |
Spastic Paraplegia 7, Autosomal Recessive; SPG7 (1 mouse model) |
| 603563 |
Spastic Paraplegia 8, Autosomal Dominant; SPG8 |
| 601162 |
Spastic Paraplegia 9, Autosomal Dominant; SPG9 |
| 601608 |
Spastic Paraplegia and Evans Syndrome |
| 607565 |
Spastic Paraplegia, Ataxia, and Mental Retardation |
| 182610 |
Spastic Paraplegia, Epilepsy, and Mental Retardation; SPEMR |
| 182830 |
Spastic Paraplegia, Optic Atrophy, and Dementia |
| 609541 |
Spastic Paraplegia, Optic Atrophy, and Neuropathy; SPOAN |
| 603117 |
Spastic Paraplegia, Optic Atrophy, Microcephaly, and XY Sex Reversal |
| 182690 |
Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy |
| 182800 |
Spastic Paraplegia with Associated Extrapyramidal Signs |
| 270805 |
Spastic Paraplegia with Myoclonic Epilepsy |
| 182815 |
Spastic Paraplegia with Neuropathy and Poikiloderma |
| 182820 |
Spastic Paraplegia with Precocious Puberty |
| 270850 |
Spastic Paresis, Glaucoma, and Mental Retardation |
| 270900 |
Spastic Pseudosclerosis |
| 270950 |
Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation |
| 313000 |
Spatial Visualization, Aptitude for |
| 245480 |
Specific Granule Deficiency; SGD |
| 606711 |
Specific Language Impairment 1; SLI1 |
| 606712 |
Specific Language Impairment 2; SLI2 |
| 607134 |
Specific Language Impairment 3; SLI3 |
| 612514 |
Specific Language Impairment 4; SLI4 |
| 182870 |
Spectrin, Beta, Erythrocytic; SPTB (2 mouse models) |
| 182875 |
Speech Development, Delayed, with Facial Asymmetry, Strabismus, and Transverse Earlobe Crease |
| 602081 |
Speech-Language Disorder 1; SPCH1 (1 mouse model) |
| 608445 |
Speech-Sound Disorder |
| 614822 |
Spermatogenic Failure 10; SPGF10 |
| 615081 |
Spermatogenic Failure 11; SPGF11 |
| 258150 |
Spermatogenic Failure 1; SPGF1 |
| 108420 |
Spermatogenic Failure 2; SPGF2 |
| 606766 |
Spermatogenic Failure 3; SPGF3 |
| 270960 |
Spermatogenic Failure 4; SPGF4 (1 mouse model) |
| 243060 |
Spermatogenic Failure 5; SPGF5 |
| 102530 |
Spermatogenic Failure 6; SPGF6 (1 mouse model) |
| 612997 |
Spermatogenic Failure 7; SPGF7 |
| 613957 |
Spermatogenic Failure 8; SPGF8 |
| 613958 |
Spermatogenic Failure 9; SPGF9 |
| 305700 |
Spermatogenic Failure, X-Linked, 1; SPGFX1 |
| 309120 |
Spermatogenic Failure, X-Linked, 2; SPGFX2 |
| 400042 |
Spermatogenic Failure, Y-Linked, 1; SPGFY1 |
| 415000 |
Spermatogenic Failure, Y-Linked, 2; SPGFY2 |
| 182882 |
Sperm Protamine P4; PRM4 |
| 601876 |
Sperm-Specific Antigen 1; SSFA1 |
| 182900 |
Spherocytosis, Type 1; SPH1 (8 mouse models) |
| 270970 |
Spherocytosis, Type 3; SPH3 (5 mouse models) |
| 612653 |
Spherocytosis, Type 4; SPH4 (1 mouse model) |
| 612690 |
Spherocytosis, Type 5; SPH5 |
| 313200 |
Spinal and Bulbar Muscular Atrophy, X-Linked 1; SMAX1 (7 mouse models) |
| 182950 |
Spinal Arachnoiditis |
| 601344 |
Spinal Dysplasia, Anhalt Type |
| 182990 |
Spinal Intradural Arachnoid Cysts |
| 604320 |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1; DSMA1 (1 mouse model) |
| 605726 |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 2; DSMA2 |
| 607088 |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3; DSMA3 |
| 611067 |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4; DSMA4 |
| 614881 |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 5; DSMA5 |
| 600175 |
Spinal Muscular Atrophy, Distal, Congenital Nonprogressive |
| 300489 |
Spinal Muscular Atrophy, Distal, X-Linked 3; SMAX3 |
| 182970 |
Spinal Muscular Atrophy, Facioscapulohumeral Type |
| 615048 |
Spinal Muscular Atrophy, Jokela Type; SMAJ |
| 182980 |
Spinal Muscular Atrophy, Late-Onset, Finkel Type; SMAFK |
| 158600 |
Spinal Muscular Atrophy, Lower Extremity, Autosomal Dominant; SMALED |
| 271200 |
Spinal Muscular Atrophy, Ryukyuan Type |
| 271220 |
Spinal Muscular Atrophy, Scapuloperoneal |
| 183020 |
Spinal Muscular Atrophy, Segmental |
| 253400 |
Spinal Muscular Atrophy, Type III; SMA3 (2 mouse models) |
| 253550 |
Spinal Muscular Atrophy, Type II; SMA2 (1 mouse model) |
| 253300 |
Spinal Muscular Atrophy, Type I; SMA1 (17 mouse models) |
| 271150 |
Spinal Muscular Atrophy, Type IV; SMA4 |
| 271225 |
Spinal Muscular Atrophy, Type I, with Congenital Bone Fractures |
| 271109 |
Spinal Muscular Atrophy with Mental Retardation |
| 271110 |
Spinal Muscular Atrophy with Microcephaly and Mental Subnormality |
| 159950 |
Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy; SMAPME |
| 301830 |
Spinal Muscular Atrophy, X-Linked 2; SMAX2 |
| 603516 |
Spinocerebellar Ataxia 10; SCA10 |
| 604432 |
Spinocerebellar Ataxia 11; SCA11 |
| 604326 |
Spinocerebellar Ataxia 12; SCA12 |
| 605259 |
Spinocerebellar Ataxia 13; SCA13 |
| 605361 |
Spinocerebellar Ataxia 14; SCA14 |
| 606658 |
Spinocerebellar Ataxia 15; SCA15 |
| 607136 |
Spinocerebellar Ataxia 17; SCA17 (4 mouse models) |
| 607458 |
Spinocerebellar Ataxia 18; SCA18 |
| 607346 |
Spinocerebellar Ataxia 19; SCA19 |
| 164400 |
Spinocerebellar Ataxia 1; SCA1 (2 mouse models) |
| 608687 |
Spinocerebellar Ataxia 20; SCA20 |
| 607454 |
Spinocerebellar Ataxia 21; SCA21 |
| 610245 |
Spinocerebellar Ataxia 23; SCA23 |
| 608703 |
Spinocerebellar Ataxia 25; SCA25 |
| 609306 |
Spinocerebellar Ataxia 26; SCA26 |
| 609307 |
Spinocerebellar Ataxia 27; SCA27 |
| 610246 |
Spinocerebellar Ataxia 28; SCA28 |
| 117360 |
Spinocerebellar Ataxia 29; SCA29 |
| 183090 |
Spinocerebellar Ataxia 2; SCA2 (2 mouse models) |
| 613371 |
Spinocerebellar Ataxia 30; SCA30 |
| 117210 |
Spinocerebellar Ataxia 31; SCA31 |
| 613909 |
Spinocerebellar Ataxia 32; SCA32 |
| 133190 |
Spinocerebellar Ataxia 34; SCA34 |
| 613908 |
Spinocerebellar Ataxia 35; SCA35 |
| 614153 |
Spinocerebellar Ataxia 36; SCA36 |
| 600223 |
Spinocerebellar Ataxia 4; SCA4 |
| 600224 |
Spinocerebellar Ataxia 5; SCA5 (1 mouse model) |
| 183086 |
Spinocerebellar Ataxia 6; SCA6 (1 mouse model) |
| 164500 |
Spinocerebellar Ataxia 7; SCA7 (6 mouse models) |
| 608768 |
Spinocerebellar Ataxia 8; SCA8 |
| 612876 |
Spinocerebellar Ataxia 9; SCA9 |
| 613728 |
Spinocerebellar Ataxia, Autosomal Recessive 10; SCAR10 |
| 614229 |
Spinocerebellar Ataxia, Autosomal Recessive 11; SCAR11 |
| 614322 |
Spinocerebellar Ataxia, Autosomal Recessive 12; SCAR12 |
| 614831 |
Spinocerebellar Ataxia, Autosomal Recessive 13; SCAR13 |
| 606002 |
Spinocerebellar Ataxia, Autosomal Recessive 1; SCAR1 |
| 213200 |
Spinocerebellar Ataxia, Autosomal Recessive 2; SCAR2 |
| 271250 |
Spinocerebellar Ataxia, Autosomal Recessive 3; SCAR3 |
| 607317 |
Spinocerebellar Ataxia, Autosomal Recessive 4; SCAR4 |
| 606937 |
Spinocerebellar Ataxia, Autosomal Recessive 5; SCAR5 |
| 608029 |
Spinocerebellar Ataxia, Autosomal Recessive 6; SCAR6 |
| 609270 |
Spinocerebellar Ataxia, Autosomal Recessive 7; SCAR7 |
| 610743 |
Spinocerebellar Ataxia, Autosomal Recessive 8; SCAR8 |
| 607250 |
Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy; (1 mouse model) |
| 271270 |
Spinocerebellar Ataxia with Dysmorphism |
| 183050 |
Spinocerebellar Ataxia with Rigidity and Peripheral Neuropathy |
| 302500 |
Spinocerebellar Ataxia, X-Linked 1; SCAX1 |
| 302600 |
Spinocerebellar Ataxia, X-Linked 2 |
| 301790 |
Spinocerebellar Ataxia, X-Linked 3 |
| 301840 |
Spinocerebellar Ataxia, X-Linked 4 |
| 300703 |
Spinocerebellar Ataxia, X-Linked 5; SCAX5 |
| 183100 |
Spinocerebellar Atrophy with Pupillary Paralysis |
| 271310 |
Spinocerebellar Degeneration and Corneal Dystrophy |
| 271320 |
Spinocerebellar Degeneration with Macular Corneal Dystrophy, Congenital Cataracts, and Myopia |
| 271322 |
Spinocerebellar Degeneration with Slow Eye Movements; SDSEM |
| 183300 |
Splenogonadal Fusion with Limb Defects and Micrognathia |
| 614979 |
Splenomegaly, Cytopenia, and Vision Loss |
| 183350 |
Splenomegaly Syndrome with Splenic Germinal Center Hypoplasia and Reduced Circulating T-Helper Cells |
| 271500 |
Splenoportal Vascular Anomalies |
| 183700 |
Split-Foot Deformity with Mandibulofacial Dysostosis |
| 183500 |
Split-Hand and Split-Foot with Hypodontia |
| 183600 |
Split-Hand/Foot Malformation 1; SHFM1 (4 mouse models) |
| 220600 |
Split-Hand/Foot Malformation 1 with Sensorineural Hearing Loss; SHFM1D |
| 313350 |
Split-Hand/Foot Malformation 2; SHFM2 |
| 246560 |
Split-Hand/Foot Malformation 3; SHFM3 (2 mouse models) |
| 605289 |
Split-Hand/Foot Malformation 4; SHFM4 |
| 606708 |
Split-Hand/Foot Malformation 5; SHFM5 |
| 225300 |
Split-Hand/Foot Malformation 6; SHFM6 |
| 119100 |
Split-Hand/Foot Malformation with Long Bone Deficiency 1; SHFLD1 |
| 610685 |
Split-Hand/Foot Malformation with Long Bone Deficiency 2; SHFLD2 |
| 612576 |
Split-Hand/Foot Malformation with Long Bone Deficiency 3; SHFLD3 |
| 183800 |
Split-Hand with Congenital Nystagmus, Fundal Changes, and Cataracts |
| 183802 |
Split-Hand with Obstructive Uropathy, Spina Bifida, and Diaphragmatic Defects |
| 183400 |
Split Lower Lip |
| 106300 |
Spondyloarthropathy, Susceptibility to, 1; SPDA1 (1 mouse model) |
| 183840 |
Spondyloarthropathy, Susceptibility to, 2; SPDA2 |
| 613238 |
Spondyloarthropathy, Susceptibility to, 3; SPDA3 |
| 600000 |
Spondylocamptodactyly |
| 272460 |
Spondylocarpotarsal Synostosis Syndrome; SCT (2 mouse models) |
| 612350 |
Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like (1 mouse model) |
| 277300 |
Spondylocostal Dysostosis 1, Autosomal Recessive; SCDO1 (2 mouse models) |
| 608681 |
Spondylocostal Dysostosis 2, Autosomal Recessive; SCDO2 |
| 609813 |
Spondylocostal Dysostosis 3, Autosomal Recessive; SCDO3 |
| 613686 |
Spondylocostal Dysostosis 4, Autosomal Recessive; SCDO4 |
| 122600 |
Spondylocostal Dysostosis 5, Autosomal Dominant; SCDO5 |
| 271520 |
Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies |
| 271550 |
Spondyloenchondrodysplasia; SPENCD |
| 607944 |
Spondyloenchondrodysplasia with Immune Dysregulation; SPENCDI |
| 612813 |
Spondyloepimetaphyseal Dysplasia, Aggrecan Type |
| 610442 |
Spondyloepimetaphyseal Dysplasia, Genevieve Type |
| 271650 |
Spondyloepimetaphyseal Dysplasia, Irapa Type; SEMDIT |
| 608728 |
Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related |
| 601096 |
Spondyloepimetaphyseal Dysplasia, Micromelic |
| 602111 |
Spondyloepimetaphyseal Dysplasia, Missouri Type |
| 602557 |
Spondyloepimetaphyseal Dysplasia, Shohat Type |
| 271510 |
Spondyloepimetaphyseal Dysplasia, Sponastrime Type |
| 184250 |
Spondyloepimetaphyseal Dysplasia, Strudwick Type; SEMDSTWK |
| 601668 |
Spondyloepimetaphyseal Dysplasia with Abnormal Dentition; SEMDAD |
| 183849 |
Spondyloepimetaphyseal Dysplasia with Hypotrichosis |
| 271640 |
Spondyloepimetaphyseal Dysplasia with Joint Laxity, Type 1; SEMDJL1 |
| 603546 |
Spondyloepimetaphyseal Dysplasia with Joint Laxity Type 2; SEMDJL2 |
| 300106 |
Spondyloepimetaphyseal Dysplasia, X-Linked |
| 300232 |
Spondyloepimetaphyseal Dysplasia, X-Linked, with Mental Deterioration |
| 611717 |
Spondyloepiphyseal Dysplasia-Brachydactyly and Distinctive Speech |
| 183900 |
Spondyloepiphyseal Dysplasia Congenita; SEDC (6 mouse models) |
| 608361 |
Spondyloepiphyseal Dysplasia, Kimberley Type |
| 184095 |
Spondyloepiphyseal Dysplasia, Maroteaux Type |
| 184000 |
Spondyloepiphyseal Dysplasia, Myopia, and Sensorineural Deafness |
| 184100 |
Spondyloepiphyseal Dysplasia Tarda, Autosomal Dominant |
| 271600 |
Spondyloepiphyseal Dysplasia Tarda, Autosomal Recessive |
| 609223 |
Spondyloepiphyseal Dysplasia Tarda, Autosomal Recessive, Leroy-Spranger Type |
| 600093 |
Spondyloepiphyseal Dysplasia Tarda with Characteristic Facies |
| 271620 |
Spondyloepiphyseal Dysplasia Tarda with Mental Retardation |
| 313400 |
Spondyloepiphyseal Dysplasia Tarda, X-Linked; SEDT |
| 600561 |
Spondyloepiphyseal Dysplasia with Atlantoaxial Instability |
| 143095 |
Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations |
| 602611 |
Spondyloepiphyseal Dysplasia with Coronal Craniosynostosis, Cataracts, Cleft Palate, and Mental Retardation |
| 183850 |
Spondyloepiphyseal Dysplasia with Punctate Corneal Dystrophy |
| 184200 |
Spondylolisthesis |
| 609616 |
Spondylomegaepiphyseal Dysplasia with Upper Limb Mesomelia, Punctate Calcifications, and Deafness |
| 613330 |
Spondylo-Megaepiphyseal-Metaphyseal Dysplasia; SMMD |
| 271665 |
Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type |
| 184253 |
Spondylometaphyseal Dysplasia, Algerian Type |
| 602271 |
Spondylometaphyseal Dysplasia, Axial |
| 184255 |
Spondylometaphyseal Dysplasia, Corner Fracture Type |
| 611702 |
Spondylometaphyseal Dysplasia, East African Type |
| 184252 |
Spondylometaphyseal Dysplasia, Kozlowski Type; SMDK |
| 250220 |
Spondylometaphyseal Dysplasia, Sedaghatian Type |
| 609052 |
Spondylometaphyseal Dysplasia, Type A4 |
| 607543 |
Spondylometaphyseal Dysplasia with Bowed Forearms and Facial Dysmorphism |
| 608940 |
Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy; SMDCRD |
| 184260 |
Spondylometaphyseal Dysplasia with Dentinogenesis Imperfecta |
| 313420 |
Spondylometaphyseal Dysplasia, X-Linked |
| 605822 |
Spondyloocular Syndrome, Autosomal Recessive |
| 271700 |
Spondyloperipheral Dysplasia |
| 184300 |
Spondylosis, Cervical |
| 601809 |
Spondylospinal Thoracic Dysostosis |
| 606688 |
Spongiform Encephalopathy with Neuropsychiatric Features |
| 184400 |
Sprengel Deformity |
| 275355 |
Squamous Cell Carcinoma, Head and Neck; HNSCC (1 mouse model) |
| 184460 |
Stapes Ankylosis with Broad Thumb and Toes |
| 248200 |
Stargardt Disease 1; STGD1 (3 mouse models) |
| 600110 |
Stargardt Disease 3; STGD3 (5 mouse models) |
| 603786 |
Stargardt Disease 4; STGD4 |
| 612948 |
Stargardt Macular Degeneration, Absent or Hypoplastic Corpus Callosum, Mental Retardation, and Dysmorphic Features |
| 184500 |
Steatocystoma Multiplex |
| 184510 |
Steatocystoma Multiplex with Natal Teeth |
| 184705 |
Steinfeld Syndrome |
| 184800 |
Sternum, Premature Obliteration of Sutures of |
| 607306 |
Steroid 5-Alpha-Reductase 2; SRD5A2 |
| 611961 |
Stevenson-Carey Syndrome |
| 184840 |
Stickler Syndrome, Type III; STL3 (1 mouse model) |
| 604841 |
Stickler Syndrome, Type II; STL2 (1 mouse model) |
| 609508 |
Stickler Syndrome, Type I, Nonsyndromic Ocular (1 mouse model) |
| 108300 |
Stickler Syndrome, Type I; STL1 |
| 614134 |
Stickler Syndrome, Type IV; STL4 |
| 614284 |
Stickler Syndrome, Type V; STL5 |
| 184850 |
Stiff-Person Syndrome; SPS (1 mouse model) |
| 184900 |
Stiff Skin Syndrome; SSKS |
| 300434 |
Stocco Dos Santos X-Linked Mental Retardation Syndrome |
| 615121 |
Stomatin-Like Protein-2, Hyperphosphorylation of |
| 185000 |
Stomatocytosis I |
| 185010 |
Stomatocytosis II |
| 185050 |
Storage Pool Platelet Disease (22 mouse models) |
| 185070 |
Stormorken Syndrome |
| 185069 |
Storm Syndrome |
| 185100 |
Strabismus, Susceptibility to |
| 185120 |
Stratton-Parker Syndrome |
| 607395 |
Streptococcus, Group A, Severity of Infection By |
| 185200 |
Striae Distensae, Familial |
| 609161 |
Striatal Degeneration, Autosomal Dominant; ADSD |
| 500003 |
Striatonigral Degeneration, Infantile, Mitochondrial |
| 271930 |
Striatonigral Degeneration, Infantile; SNDI |
| 601367 |
Stroke, Ischemic |
| 606799 |
Stroke, Susceptibility to, 1 |
| 185300 |
Sturge-Weber Syndrome; SWS |
| 184450 |
Stuttering, Familial Persistent, 1; STUT1 |
| 609261 |
Stuttering, Familial Persistent, 2; STUT2 |
| 614655 |
Stuttering, Familial Persistent, 3; STUT3 |
| 614668 |
Stuttering, Familial Persistent, 4; STUT4 |
| 601559 |
Stuve-Wiedemann Syndrome |
| 271950 |
Subaortic Stenosis, Membranous |
| 271960 |
Subaortic Stenosis--Short Stature Syndrome |
| 600335 |
Succinic Acidemia |
| 271980 |
Succinic Semialdehyde Dehydrogenase Deficiency; SSADHD (1 mouse model) |
| 245050 |
Succinyl-Coa:3-Oxoacid Coa Transferase Deficiency |
| 222900 |
Sucrase-Isomaltase Deficiency, Congenital; CSID |
| 272000 |
Sucrosuria, Hiatus Hernia and Mental Retardation |
| 272100 |
Sudanophilic Cerebral Sclerosis |
| 272120 |
Sudden Infant Death Syndrome (1 mouse model) |
| 608800 |
Sudden Infant Death with Dysgenesis of the Testes Syndrome; SIDDT |
| 272150 |
Sugarman Brachydactyly |
| 185460 |
Sulfhemoglobinemia, Congenital |
| 272300 |
Sulfocysteinuria |
| 272350 |
Summitt Syndrome |
| 601708 |
Superior Transverse Scapular Ligament, Calcification of, Familial |
| 613700 |
Supernumerary Der(22)t(8;22) Syndrome |
| 191181 |
Suppressor of Tumorigenicity 3; ST3 |
| 185480 |
Suprabulbar Paresis, Congenital |
| 601104 |
Supranuclear Palsy, Progressive, 1; PSNP1 |
| 609454 |
Supranuclear Palsy, Progressive, 2; PSNP2 |
| 610898 |
Supranuclear Palsy, Progressive, 3; PSNP3 |
| 185500 |
Supravalvular Aortic Stenosis; SVAS (2 mouse models) |
| 185540 |
Surface Antigen, Glycoprotein 75 |
| 185610 |
Surface Polypeptides, Anonymous |
| 265120 |
Surfactant Metabolism Dysfunction, Pulmonary, 1; SMDP1 (4 mouse models) |
| 610913 |
Surfactant Metabolism Dysfunction, Pulmonary, 2; SMDP2 |
| 610921 |
Surfactant Metabolism Dysfunction, Pulmonary, 3; SMDP3 (3 mouse models) |
| 300770 |
Surfactant Metabolism Dysfunction, Pulmonary, 4; SMDP4 |
| 614370 |
Surfactant Metabolism Dysfunction, Pulmonary, 5; SMDP5 |
| 108985 |
Sveinsson Chorioretinal Atrophy; SCRA |
| 185650 |
Symphalangism, C. S. Lewis Type |
| 185700 |
Symphalangism, Distal |
| 606895 |
Symphalangism, Distal, with Microdontia, Dental Pulp Stones, and Narrowed Zygomatic Arch |
| 185600 |
Symphalangism of Toes |
| 185800 |
Symphalangism, Proximal; SYM1 |
| 185750 |
Symphalangism with Multiple Anomalies of Hands and Feet |
| 609289 |
Syncope, Familial Vasovagal; VVS |
| 609432 |
Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction; MSSD |
| 186350 |
Syndactyly-Polydactyly-Earlobe Syndrome |
| 185900 |
Syndactyly, Type I |
| 186100 |
Syndactyly, Type III |
| 186200 |
Syndactyly, Type IV |
| 272440 |
Syndactyly, Type I, with Microcephaly and Mental Retardation |
| 186300 |
Syndactyly, Type V |
| 272450 |
Syndesmodysplasic Dwarfism |
| 612759 |
Synesthesia |
| 119550 |
Syngnathia |
| 186400 |
Synostoses, Tarsal, Carpal, and Digital |
| 186575 |
Synovial Chondromatosis, Familial, with Dwarfism |
| 186000 |
Synpolydactyly 1; SPD1 (3 mouse models) |
| 608180 |
Synpolydactyly 2; SPD2 |
| 610234 |
Synpolydactyly 3; SPD3 |
| 186600 |
Syringomas, Multiple |
| 186700 |
Syringomyelia, Isolated |
| 614420 |
Systemic Lupus Erythematosus 16; SLEB16 |
| 152700 |
Systemic Lupus Erythematosus; SLE (46 mouse models) |
| 612251 |
Systemic Lupus Erythematosus, Susceptibility to, 10; SLEB10 |
| 612253 |
Systemic Lupus Erythematosus, Susceptibility to, 11; SLEB11 |
| 612254 |
Systemic Lupus Erythematosus, Susceptibility to, 12; SLEB12 |
| 612378 |
Systemic Lupus Erythematosus, Susceptibility to, 13; SLEB13 |
| 613145 |
Systemic Lupus Erythematosus, Susceptibility to, 14; SLEB14 |
| 300809 |
Systemic Lupus Erythematosus, Susceptibility to, 15; SLEB15 |
| 601744 |
Systemic Lupus Erythematosus, Susceptibility to, 1; SLEB1 |
| 605218 |
Systemic Lupus Erythematosus, Susceptibility to, 2; SLEB2 (3 mouse models) |
| 605480 |
Systemic Lupus Erythematosus, Susceptibility to, 3; SLEB3 |
| 608437 |
Systemic Lupus Erythematosus, Susceptibility to, 4; SLEB4 |
| 609903 |
Systemic Lupus Erythematosus, Susceptibility to, 5; SLEB5 |
| 609939 |
Systemic Lupus Erythematosus, Susceptibility to, 6; SLEB6 |
| 610065 |
Systemic Lupus Erythematosus, Susceptibility to, 7; SLEB7 |
| 610066 |
Systemic Lupus Erythematosus, Susceptibility to, 8; SLEB8 |
| 610927 |
Systemic Lupus Erythematosus, Susceptibility to, 9; SLEB9 |
| 607279 |
Systemic Lupus Erythematosus with Hemolytic Anemia, Susceptibility to, 1; SLEH1 |
| 607965 |
Systemic Lupus Erythematosus with Nephritis, Susceptibility to, 1; |
| 607966 |
Systemic Lupus Erythematosus with Nephritis, Susceptibility to, 2; |
| 607967 |
Systemic Lupus Erythematosus with Nephritis, Susceptibility to, 3; |
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