Disease Index
9,486 diseasesStickler syndrome type 2
human disease
MeSH: C537493
Stickler syndrome type 3
MeSH: C537494
Stiff Person Syndrome
Stiff person syndrome is a rare autoimmune neurological disorder characterized by progressive muscle rigidity, painful spasms, and heightened sensitivity to stimuli. Most cases are associated with anti-glutamic acid decarboxylase (anti-GAD) antibodies, though anti-amphiphysin and anti-glycine receptor antibodies are found in paraneoplastic variants. The estimated prevalence is approximately 1-2 per million, with a 2:1 female predominance.
ICD: G25.82MeSH: D016750
stiff skin syndrome
medical condition
ICD: Q82.8MeSH: C566112
Stimmler syndrome
medical condition
MeSH: C565968
STING-associated vasculopathy with onset in infancy
rare autoinflammatory condition
stomach cancer
gastrointestinal system cancer that is located in the stomach
stomach carcinoma
stomach cancer that is located in the stomach
stomach polyp
polyp that arises from the stomach. This category includes neoplastic polyps (intestinal-type adenomatous polyps, gastric-type adenomas, and fundic gland polyps), and non-neoplastic polyps (hyperplastic polyps and hamartomatous polyps)
MeSH: C562464
Stormorken syndrome
Human disease
MeSH: C566108
Straddling and/or overriding mitral valve
human disease
Straddling or overriding tricuspid valve
human disease
Stratton Parker syndrome
medical condition
MeSH: C566105
streptococcal toxic shock-like syndrome
stress polycythemia
Human disease
striatal degeneration, autosomal dominant
human disease
MeSH: C563783
Striate palmoplantar keratoderma
stromal dystrophy
Human disease
stromal keratitis
Stromme syndrome
human disease
MeSH: C565460
strongyloidiasis
Human helminthiasis
MeSH: D013322
Sturge–Weber syndrome
neurological and skin disorder associated with port-wine stains of the face, glaucoma, seizures, intellectual disability, and cerebral malformations
ICD: Q85.8MeSH: D013341
Stüve-Wiedemann syndrome
human disease
MeSH: C537502
sub-cortical nodular heterotopia
human disease
subacute cutaneous lupus erythematosus
medical condition
ICD: L93.1
subacute inflammatory demyelinating polyneuropathy
subacute sclerosing panencephalitis
rare insidious sequela from measles infection
ICD: A81.1MeSH: D013344
subaortic course of innominate vein
human disease
subaortic stenosis-short stature syndrome
human disease
MeSH: C537749
subcorneal pustular dermatosis
human disease