Rare Disease Index
9,491 diseasessmall intestine adenocarcinoma
small intestine carcinoma that derives from epithelial cells of glandular origin
small intestine carcinoma
small intestine cancer that develops from epithelial cells and is located in the small intestine
small intestine leiomyosarcoma
small intestine sarcoma that affects the involuntary smooth muscles of the small intestines
small intestine neuroendocrine neoplasm
human disease
Smarca4-deficient sarcoma of thorax
human disease
SMARCA4-deficient sarcoma of thorax
human disease
Smith-Lemli-Opitz syndrome
an inborn error of cholesterol synthesis, caused by a mutation in the enzyme 7-Dehydrocholesterol reductase
MeSH: D019082
Smith-Magenis syndrome
Human disease
MeSH: D058496
Smith-McCort dysplasia
osteochondrodysplasia characterized by short limbs and a short trunk with a barrel-shaped chest and has material basis in homozygous or compound heterozygous mutation in the DYM gene on chromosome 18q
MeSH: C564589
Smith–Fineman–Myers syndrome
medical condition
MeSH: C537445
Smouldering systemic mastocytosis
snakebite
injury caused by a bite from a snake
ICD: T63.0MeSH: D012909
Sneddon syndrome
form of arteriopathy
ICD: M30.8MeSH: D018860
Snijders Blok-Campeau syndrome
medical condition
snowflake vitreoretinal degeneration
MeSH: C536677
Snyder-Robinson syndrome
Human disease
MeSH: C536678
sodium channelopathy-related small fiber neuropathy
human disease
sodoku
medical condition
ICD: A25.0
soft tissue neoplasm
neoplasm that arises from soft tissue
MeSH: D012983
soft-tissue sarcoma
human disease
solar urticaria
skin disease
ICD: L56.3MeSH: D000092130
solid pseudopapillary tumour
medical condition
solid tumor associated with an acquired peripheral neuropathy
human disease
solitary mastocytoma
Human disease
MeSH: D054705
solitary median maxillary central incisor syndrome
human disease
MeSH: C537342
solitary necrotic nodule of the liver
solitary rectal ulcer syndrome
ICD: K62.6
Somatomammotropinoma
human disease
somatostatinoma
Human disease
MeSH: D013005
Sorsby's fundus dystrophy
human disease
MeSH: C564992