Disease Index
9,486 diseasescryptorchidism-arachnodactyly-intellectual disability syndrome
medical condition
cryptosporidiosis
Human disease
ICD: A07.207.2MeSH: D003457
cryptosporidiosis-chronic cholangitis-liver disease syndrome
human disease
curly hair-acral keratoderma-caries syndrome
MeSH: C536220
Currarino syndrome
medical condition
MeSH: C536221
Curry-Jones syndrome
medical condition
Cushing syndrome due to macronodular adrenal hyperplasia
human disease
MeSH: C565662
Cushing's disease
disease related to the anterior pituitary
ICD: E24.0
Cushing's syndrome
adrenal gland overactivity caused by a tumor of the pituitary gland or by medication
MeSH: D003480
cutaneous B-cell lymphoma
human disease
cutaneous collagenous vasculopathy
Cutaneous collagenous vasculopathy (CCV) is a primary microangiopathy confined to the skin, characterized by multiple and widespread telangiectasias
cutaneous larva migrans
medical condition
ICD: B76.9MeSH: D007815
cutaneous lupus erythematosus
lupus erythematosus that causes skin lesions on parts of the body that are exposed to sunlight
MeSH: D008178
cutaneous lymphoid hyperplasia
pseudolymphoma of the skin
ICD: L98.8
cutaneous lymphoma
medical condition
cutaneous mastocytosis
human disease
MeSH: D034701
cutaneous photosensitivity-lethal colitis syndrome
MeSH: C536224
cutaneous polyarteritis nodosa
cutaneous small-vessel vasculitis
hypersensitivity vasculitis that results in inflammation of small blood vessels, characterized clinically by palpable purpura, which is a slightly elevated purpuric rash over one or more areas of the skin
cutaneous T cell lymphoma
non-Hodgkin's lymphoma that has material basis in a mutation of T cells
ICD: C84.0MeSH: D016410
cutis laxa
skin disease characterized by skin that is loose, hanging, wrinkled and lacking in elasticity; it can also affect connective tissue in other parts of the body, including the heart, blood vessels, joints, intestines and lungs
MeSH: D003483
cutis laxa-marfanoid syndrome
human disease
MeSH: C563639
cutis marmorata telangiectatica congenita
medical condition
ICD: L95.0MeSH: C536226
Cutis verticis gyrata
medical condition
cutis verticis gyrata mental deficiency
human disease
cyanide poisoning
broad-spectrum poisoning by inhibition of the aerobic respiration metabolism at the cellular level in mitochondria
ICD: T65.0
cyanide-induced parkinsonism
human disease
cyclic hematopoiesis
Human disease
MeSH: C536227
cyclosporiasis
infection caused by Cyclospora cayetanensis
MeSH: D021866
cylindrical spirals myopathy
Human disease
MeSH: C563535