Disease Index

9,486 diseases
sporotrichosis
fungal infection caused by Sporothrix schenckii
MeSH: D013174
spotted fever
Human disease
MeSH: D000073605
Sprengel's deformity
human disease
ICD: Q74.0MeSH: C535802
squamous cell carcinoma of gallbladder and extrahepatic biliary tract
human disease
squamous cell carcinoma of liver and intrahepatic biliary tract
human disease
squamous cell carcinoma of pancreas
squamous cell carcinoma that involves the pancreas
squamous cell carcinoma of the corpus uteri
squamous cell carcinoma that involves the body of uterus
squamous cell carcinoma of the oral tongue
human disease
squamous cell carcinoma of the small intestine
carcinoma that arises from the small intestine. It is composed of malignant squamous cells
St. Louis encephalitis
human disease
ICD: A83.3MeSH: D004674
staphylococcal necrotizing pneumonia
staphylococcal toxemia
human disease
staphylococcal toxic-shock syndrome
STAR syndrome
This syndrome is characterised by the association of toe syndactyly, facial dysmorphism including telecanthus (abnormal distance between the eyes) and a broad nasal tip, urogenital malformations and anal atresia
MeSH: C567475
Stargardt disease
age related macular degeneration that is characterized by progressive vision loss usually to the point of legal blindness
ICD: H35.5MeSH: D000080362
startle epilepsy
seizures triggered by sudden sensory stimuli, mostly auditory
STAT3-related early-onset multisystem autoimmune disease
human disease
steatocystoma multiplex
disease
ICD: L72.2MeSH: D062685
steatocystoma multiplex-natal teeth syndrome
The syndrome steatocystoma multiplex and natal teeth is characterized by generalized multiple steatocystomas and natal teeth
MeSH: C537487
Steel syndrome
human disease
Steinfeld syndrome
Holoprosencephaly-radial heart renal anomalies syndrome is characterised by holoprosencephaly, predominantly radial limb deficiency (absent thumbs, phocomelia), heart defects, kidney malformations and absence of gallbladder
MeSH: C566655
stenosis or atrophy of the coronary ostium
human disease
Sternal cleft
medical condition
MeSH: C537489
sternocostoclavicular hyperostosis
rare, benign rheumatologic disorder or syndrome characterized by hyperostosis and soft tissue ossification between the clavicles and the anterior part of the upper ribs
MeSH: D015218
sterol biosynthesis disorder
acquired metabolic disease that is has its basis in the disruption of sterol biosynthetic process
sterol metabolism disorder
acquired metabolic disease that is has its basis in the disruption of sterol metabolic process
sterol metabolism disorder with epilepsy
human disease
Stevens–Johnson syndrome
skin disease
MeSH: D013262
Stickler syndrome
rare genetic disorder affecting collagen
ICD: Q89.8MeSH: C537492
Stickler syndrome type 1
human disease
MeSH: C537492
Page 285 of 317 (9,486 total)