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List of all diseases starting with S

• S-ADENOSYLHOMOCYSTEINE HYDROLASE DEFICIENCY (SAHH) MIM=613752
• SALLA DISEASE MIM=604369
• SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME (SPDRS) MIM=609056
• SARCOSINEMIA MIM=268900
• SC4MOL DEFICIENCY MIM=616834
• SCHINDLER DISEASE, TYPE I MIM=609241
• SCHNECKENBECKEN DYSPLASIA (CDG) MIM=269250
• SEDOHEPTULOKINASE DEFICIENCY (SHPKD) MIM=612713
• SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE (SESAMES) MIM=612780
• SELENIUM DEFICIENCY MIM=
• SENGERS SYNDROME MIM=212350
• SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS (SANDO) MIM=607459
• SEPSIS, NEONATAL [DD] MIM=---
• SERINE DEFIENCY SYNDROME (NEW DISEASE?) MIM=
• SEVERE COMBINED IMMUNODEFICIENCY (SCID) MIM=
• SHORT CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY (SCAD) MIM=201470
• SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS (SDDHD, TKT) MIM=617044
• SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (SOPH) MIM=614800
• SIALIC ACID STORAGE DISEASE, INFANTILE TYPE MIM=269920
• SIALIDOSIS TYPE I MIM=256550
• SIALIDOSIS TYPE II MIM=256550
• SIALURIA MIM=269921
• SMITH-LEMLI-OPITZ SYNDROME (SLOS) MIM=270400
• SOLUTE CARRIER FAMILY 28 (SODIUM-COUPLED NUCLEOSIDE TRANSPORTER), MEMBER 1; SLC28A1 MIM=606207
• SOLUTE CARRIER FAMILY 5 (SODIUM-DEPENDENT VITAMIN TRANSPORTER), MEMBER 6 (SLC5A6) MIM=604024
• SORBITOL DEHYDROGENASE (DEFICIENCY) MIM=182500
• SOTOS SYNDROME 1; SOTOS1 MIM=117550
• SOTOS SYNDROME 2; SOTOS2 MIM=614753
• SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE; SPAX5 MIM=614487
• SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE; SACS MIM=270550
• SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE (SPG28) MIM=609340
• SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (SPG5A) MIM=270800
• SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT (SPG73) MIM=616282
• SPASTIC PARAPLEGIA 82, AUTOSOMAL RECESSIVE (SPG82) MIM=618770
• SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT (SPG9A) MIM=601162
• SPASTIC PARAPLEGIA, EPILEPSY, AND MENTAL RETARDATION (SPEMR) MIM=182610
• SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20 (SNX14) MIM=616354
• SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25; SCAR25 MIM=617584
• SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY 3 (SCAN3) MIM=618387
• SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE (SCE-EDS) MIM=612350
• SPONDYLOCOSTAL DYSOSTOSIS 3, AUTOSOMAL RECESSIVE (SCDO3) MIM=609813
• SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE (SMDS) MIM=250220
• SQUALENE SYNTHASE DEFICIENCY MIM=618156
• SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY (SSADH) MIM=271980
• SUCCINYL CoA: 3-KETOACID CoA TRANSFERASE DEFICIENCY (SCOT) MIM=245050
• SUCRASE-ISOMALTASE DEFICIENCY MIM=222900
• SUDDEN CARDIAC FAILURE, INFANTILE (SCFI) MIM=617222
• SULFIDE QUINONE OXIDOREDUCTASE DEFICIENCY (SQOR) (NEW DISEASE?) MIM=617658
• SULFITE OXIDASE DEFICIENCY (SOD) MIM=272300
• SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1 MIM=265120
• SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2; SMDP2 MIM=610913