Disease Index
9,486 diseasescongenital enteropathy involving intestinal mucosa development
human disease
congenital enterovirus infection
human disease
congenital entropion
human disease
congenital Epstein-Barr virus infection
congenital epulis
Human disease
congenital erosive and vesicular dermatosis
human disease
congenital erythropoietic porphyria
congenital human disease
MeSH: D017092
congenital esophageal diverticulum
congenital eyelid retraction
Congenital eyelid retraction is a very rare kinetic eyelid anomaly that can affect the upper or lower eyelid, presents at birth, that in some cases can result in corneal exposure, and that may be associated with accessory levator muscle slips
congenital facial paralysis
human disease
congenital fiber-type disproportion
Human disease
Congenital fourth nerve palsy
human disease
ICD: H49.1MeSH: C565007
congenital generalized hypercontractile muscle stiffness syndrome
human disease
congenital generalized lipodystrophy type 4
congenital generalized lipodystrophy that has material basis in an autosomal recessive mutation of PTRF on chromosome 17q21.2
congenital genu flexum
human disease
congenital heart block
atrioventricular block characterized by the presence of conduction system disease of any form, which is diagnosed on or before 28 days of life
ICD: Q24.6MeSH: C535758
congenital heart defect-round face-developmental delay syndrome
medical condition
MeSH: C536680
congenital heart disease
cardiovascular disease
MeSH: D006330
congenital hemangioma
hemangioma present and fully formed at birth. The different types are Rapidly involuting congenital hemangiomas (RICH), Partially involuting congenital hemangioma (PICH) and Non-involuting congenital hemangiomas (NICH)
congenital hemolytic anemia
human disease
MeSH: D000745
congenital hereditary endothelial dystrophy of cornea
Human disease
MeSH: C536439
congenital hereditary endothelial dystrophy type I
congenital hereditary facial paralysis-variable hearing loss syndrome
congenital high-molecular-weight kininogen deficiency
rare autosomal recessive inherited disorder characterized by prolonged partial thromboplastin time and absence of bleeding diathesis
MeSH: C537060
congenital Horner syndrome
human disease
MeSH: C564178
congenital hydrocephalus
Hydrocephalus that is present at birth
congenital hydronephrosis
congenital hyperinsulinism
genetic disease
MeSH: D044903
Congenital hypofibrinogenemia
Familial hypofibrinogenemia is a coagulation disorder characterized by mild bleeding symptoms following trauma or surgery due to a reduced plasma fibrinogen concentration
Congenital hypopituitarism
human disease
ICD: Q89.2