Disease Index
9,486 diseasesCorneal-cerebellar syndrome
medical condition
MeSH: C535472
Cornelia de Lange syndrome
genetic disease
MeSH: D003635
Corneodermatoosseous syndrome
Autosomal dominant condition causing eye and skeletal problems
MeSH: C536444
corneogoniodysgenesis
human disease
corneoiridogoniodysgenesis
human disease
coronary arterial fistula
Coronary arterial fistulas are a connection between one or more of the coronary arteries and a cardiac chamber or great vessel
coronary artery anomaly
Human disease
ICD: Q24.5MeSH: D003330
coronary artery intramyocardial course
human disease
coronary sinus atresia
human disease
coronary sinus stenosis
human disease
coronin-1A deficiency
severe combined immunodeficiency that is an actin regulator when mutated results in SCID through inhibition of thymic egress of mature thymocytes into peripheral lymphoid organs
corpus callosum agenesis-abnormal genitalia syndrome
medical condition
MeSH: C563110
corpus callosum agenesis-double urinary collecting system syndrome
human disease
MeSH: C535427
corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome
Human disease
MeSH: C564509
corpus callosum agenesis-macrocephaly-hypertelorism syndrome
human disease
corpus callosum dysgenesis hypopituitarism
human disease
cortical blindness-intellectual disability-polydactyly syndrome
This syndrome is characterised by cortical blindness, intellectual deficit, and polydactyly
MeSH: C565674
cortical dysplasia-focal epilepsy syndrome
brain disease characterized by cortical dysplasia, focal epilepsy, macrocephaly, and diminished deep-tendon reflexes that has material basis in homozygous or compound heterozygous mutation in the CNTNAP2 gene on chromosome 7q35-q36
corticobasal degeneration
progressive neurodegenerative condition affecting the cerebral cortex and basal ganglia
MeSH: D000088282
corticobasal syndrome
rare neurodegenerative disease
corticosteroid-binding globulin deficiency
human disease
Corticosteroid-sensitive aseptic abscess syndrome
Corticosteroid-sensitive aseptic abscesses syndrome is a well-defined entity within the group of autoinflammatory disorders
cortisone reductase deficiency
endocrine system disease characterized by failure to regenerate the active glucocorticoid cortisol from cortisone resulting in adrenal hyperandrogenism
MeSH: C536447
Costello syndrome
syndrome characterized by craniofacial dysmorphology, cardiac defects, mild intellectual disability, and high birth weight followed by a failure to thrive and developmental delays
MeSH: D056685
Cote Katsantoni syndrome
human disease
MeSH: C536449
Cousin syndrome
genetic disorder
MeSH: C535550
Cousin–Walbraum–Cegarra syndrome
medical condition
Cowden syndrome 1
inherited disorder causing tumor-like growth and increased cancer risk
Coxoauricular syndrome
MeSH: C565148
Crandall syndrome
medical condition