Disease Index

9,486 diseases
keratosis follicularis-dwarfism-cerebral atrophy syndrome
medical condition
MeSH: C536158
Keratosis linearis with ichthyosis congenital and sclerosing keratoderma syndrome
medical condition
MeSH: C566600
keratosis palmaris et plantaris-clinodactyly syndrome
MeSH: C563646
keratosis pilaris atrophicans
human disease
ICD: L85.8
keratosis pilaris atrophicans faciei
human disease
kerion
fungal infection
ICD: B35.0MeSH: C536165
kernicterus
congenital disorder of nervous system
MeSH: D007647
ketamine-induced biliary dilatation
ketoacidosis due to monocarboxylate transporter-1 deficiency
human disease
Keutel syndrome
Keutel syndrome is characterised by diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism
MeSH: C536167
kidney clear cell sarcoma
kidney sarcoma that has material basis in clear cells that are characterized as cells that look clear when viewed under a microscope
kidney disease
urinary system disease that is located in the kidney
MeSH: D007674
Kienbock's disease
Kienbock disease is a rare bone disorder of unknown etiology characterized clinically by osteonecrosis of the carpal lunate, eventually leading to collapse of the lunate bone impacting wrist function
ICD: M87.9
Kikuchi disease
rare disease
MeSH: D020042
Kimura disease
Human disease
ICD: I89.8MeSH: D000082242
Kindler syndrome
skin disease characterized by congenital blistering, skin atrophy, photosensitivity, skin fragility, and scaling
ICD: Q82.8MeSH: C536321
kinetic eyelid anomaly
human disease
King-Denborough syndrome
MeSH: C536883
Kjer's optic neuropathy
medical condition
Klatskin's tumor
Human disease
ICD: C24.0MeSH: D018285
Kleefstra syndrome
Human disease
ICD: Q93.5MeSH: C563043
Kleefstra syndrome 2
human disease
Kleefstra syndrome due to 9q34 microdeletion
human disease
Kleefstra syndrome due to a point mutation
human disease
Kleine-Levin syndrome
recurrent hypersomnia that is characterized by recurring periods of excessive amounts of sleep and altered behavior
ICD: G47.8MeSH: D017593
KLHL9-related early-onset distal myopathy
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome
human disease
Klippel-Feil syndrome
physical disorder that has material basis in abnormal segmentation of the vertebra during fetal development which results in fusion located in cervical vertebra
MeSH: D007714
Klippel–Trénaunay–Weber syndrome
syndrome that is characterized by large cutaneous hemangiomata with hypertrophy of the related bones and soft tissues
MeSH: D007715
Klüver–Bucy syndrome
syndrome resulting from bilateral lesions of the medial temporal lobe
ICD: F07.0MeSH: D020232
Page 168 of 317 (9,486 total)