Disease Index

9,486 diseases
connective tissue disorder due to lysyl hydroxylase-3 deficiency
MeSH: C567320
cono-spondylar dysplasia
human disease
conotruncal heart malformations
human disease
MeSH: C535464
constitutional anemia due to iron metabolism disorder
human disease
constitutional deficiency anemia
human disease
constitutional dyserythropoietic anemia
human disease
constitutional hemolytic anemia due to acanthocytosis
human disease
constitutional megaloblastic anemia due to folate metabolism disorder
human disease
constitutional megaloblastic anemia with severe neurologic disease
human disease
MeSH: C565095
constitutional neutropenia
rare disorder characterized by recurrent infantile infections and absence of neutrophils in the peripheral blood
constitutional neutropenia with extra-hematopoietic manifestations
human disease
constitutional thrombocytopenia
human disease
continuous spikes and waves during sleep
contractures-developmental delay-Pierre robin syndrome
human disease
contractures-ectodermal dysplasia-cleft lip/palate syndrome
MeSH: C535465
Contractures-webbed neck-micrognathia-hypoplastic nipples syndrome
human disease
Cooks syndrome
rare congenital malformation syndrome
MeSH: C537766
Cooper-Jabs syndrome
MeSH: C565923
Copenhagen disease
Progressive non-infectious anterior vertebral fusion (PAVF) is an early childhood spinal disorder characterized by the gradual onset of thoracic and/or lumbar spine ankylosis often in conjunction with kyphosis with distinctive radiological features
copper metabolism disease
Human disease
ICD: E83.0
cor triatriatum
congenital heart defect where the left atrium (cor triatriatum sinistrum) or right atrium (cor triatriatum dextrum) is subdivided by a thin membrane, resulting in three atrial chambers
ICD: Q24.2MeSH: D003310
cor triatriatum dexter
human disease
cor triatriatum sinister
coralliform cataract
human disease
cordiform uterus
human disease
cornea plana
Human disease
Cornea plana 1
congenital hereditary deformity of the eye surface
ICD: Q13.4
Cornea plana 2
medical condition
ICD: Q13.4
corneal dystrophy
human disease
ICD: H18.5MeSH: D003317
corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome
human disease
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