Disease Index
9,486 diseasessecondary interstitial lung disease specific to childhood associated with a systemic vasculitis
human disease
secondary intestinal lymphangiectasia
secondary neonatal autoimmune disease
human disease
secondary non-traumatic avascular necrosis
human disease
secondary polyarteritis nodosa
Secondary polyarteritis nodosa (PAN) is a rare serious form of PAN (see this term) characterized by vasculitis in a background of viral infection, primarily with hepatitis B virus (HBV)
secondary pulmonary alveolar proteinosis
form of pulmonary alveolar proteinosis that arises in association with hematological disorders, medications, certain infections, acute silicosis, and immunodeficiency
secondary pulmonary hemosiderosis
secondary sclerosing cholangitis
human disease
secondary short bowel syndrome
Secondary short bowel syndrome is an intestinal failure caused by any condition that results in a functional small intestine of less than 200 cm in length and is characterized by diarrhea, nutrient malabsoption, bowel dilation and dysmobility
secondary syringomyelia
human disease
secondary vasculitis
human disease
secretory apparatus of the lacrimal system anomaly
human disease
secretory component deficiency
human disease
MeSH: C562869
Segmental odontomaxillary dysplasia
segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome
human disease
segmental progressive overgrowth syndrome with fibroadipose hyperplasia
human disease
seizures-intellectual disability due to hydroxylysinuria syndrome
MeSH: C565502
seizures-scoliosis-macrocephaly syndrome
human disease
selective IgM deficiency disease
selective immunoglobulin deficiency disease thatis a dysgammaglobulinemia resulting from decreased levels of immunoglobulin M (IgM) production to roduction of other antibodies
ICD: D80.4
selective pituitary resistance to thyroid hormone
human disease
MeSH: C564154
Self-healing papular mucinosis
medical condition
semantic dementia
progressive neurodegenerative disorder
Semilobar holoprosencephaly
Semilobar holoprosencephaly is one of the classical forms of holoprosencephaly (HPE; see this term) in which the left and right frontal and parietal lobes are fused and the interhemispheric fissure is only present posteriorly
Sengers syndrome
Human disease
MeSH: C538280
Senior-Boichis syndrome
Senior-Loken syndrome
autosomal recessive genetic disease characterized by progressive wasting of the filtering unit of the kidney (nephronophthisis), with or without medullary cystic renal disease, and progressive eye disease
MeSH: C537580
Sensenbrenner syndrome
Human disease
ICD: Q87.5
sensorineural hearing loss-early graying-essential tremor syndrome
Sensorineural hearing loss-early graying-essential tremor syndrome is characterised by the combination of sensorineural hearing loss, early greying of scalp hair and adult onset essential tremor
sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome is characterised by adult-onset severe sensory ataxic neuropathy, dysarthria and chronic progressive external ophthalmoplegia
MeSH: C537583
Senter syndrome
medical condition