disease
abnormal condition negatively affecting organisms
corneal ulcer
area of epithelial tissue loss from corneal surface; associated with inflammatory cells in the cornea and anterior chamber
hyperkeratosis
thickening of the stratum corneum (the outermost layer of the epidermis), often associated with the presence of an abnormal quantity of keratin
postoperative nausea and vomiting
medical condition
receptive aphasia
type of aphasia
Carrion's disease
infectious disease produced by Bartonella bacilliformis infection
medication overuse headache
medical condition
deep vein thrombosis
formation of a blood clot (thrombus) in a deep vein
medullary cystic kidney disease
inherited form of cystic kidney disease leading to fibrosis and impaired renal function that is caused by mutations in the UMOD gene, which encodes uromodulin/Tamm-Horsfall mucoprotein
Castleman's disease
lymphoproliferative syndrome characterized by one or more enlarged lymph nodes containing cells with hyaline-vascular, plasmacytic, or mixed appearance microscopically
Myeloma cast nephropathy
medical condition
enterobiasis
parasitic disease
sympathetic ophthalmia
Human disease
eosinophilic esophagitis
esophagitis characterized by inflammation involving eosinophils located in esophagus
Silver-Russell syndrome
growth disorder
substance-induced psychosis
a psychosis that results from the effects of exogenous toxic substances or drugs
abdominal aortic aneurysm
aortic aneurysm that is located in the abdominal aorta
Sjogren-Larsson syndrome
autosomal recessive form of ichthyosis apparent at birth
scaphocephaly
premature fusion of the sagittal suture
Riley-Day syndrome
hereditary sensory and autonomic neuropathy type III (HSAN-III), is a disorder of the autonomic nervous system which affects the development and survival of sensory
stenosis
abnormal narrowing of a blood vessel or other tubular organ or structure; also sometimes called a stricture
absence seizure
generalized seizure characterized by a brief loss and return of consciousness, generally not followed by a period of lethargy
Canavan disease
neurodegenerative disorder; its spectrum varies between severe forms with leukodystrophy, macrocephaly and severe developmental delay, and a very rare mild/juvenile form characterized by mild developmental delay
delusional misidentification syndrome
psychopathological syndrome
virilism
development of male secondary sex characteristics in the female
Ramsay Hunt syndrome
unrelated neurological syndromes described by James Ramsay Hunt
contagious disease
subset category of transmissible diseases, which are transmitted to other persons
congenital insensitivity to pain
medical condition
endemic typhus
typhus transmitted by fleas (Xenopsylla cheopis), usually on rats
developmental disorder
disease of mental health that occur during a child's developmental period between birth and age 18 resulting in retarding of the child's psychological or physical development
hypervitaminosis A
Human disease
pain disorder
somatoform disorder that involves chronic pain in one or more areas, and is thought to be caused by psychological stress.
familial amyloid neuropathy
human disease
neurological disorder
disease of an anatomical entity located in the central or peripheral nervous system
prurigo
medical condition
organic personality disorder
mental disorder
slipping rib syndrome
medical condition
obstructive symptoms
kind of lower urinary tract symptoms
sensory processing differences
neurodevelopmental differences involving heightened and/or muted responses to sensory input
first-degree atrioventricular block
disease of the electrical conduction system of the heart in which the PR interval is lengthened beyond 0.20 seconds
keratosis
skin disease characterized by growth of keratin on the skin or mucous membranes
lymphocytic interstitial pneumonia
medical condition
hepatic porphyria
form of porphyria in which the enzyme deficiency occurs in the liver
parathyroid adenoma
Human disease