congenital heart defect-round face-developmental delay syndrome
Also known as: Sonoda syndrome, round face with depressed nasal Bridge and small mouth, congenital heart defect, and retarded development
Additional Disease Briefs
congenital heart defects, multiple types, 2
Also known as: CHTD2, TAB2 congenital heart malformation, congenital heart defects, multiple types, 2, congenital heart defects, nonsyndromic, 2, congenital heart malformation caused by mutation in TAB2
congenital heart defects, multiple types, 4
Also known as: CHTD4, NR2F2 congenital heart defects, multiple types, congenital heart defects, multiple types caused by mutation in NR2F2, congenital heart defects, multiple types, 4
congenital heart defects, multiple types, 6
Also known as: CHTD6, DTGA3, GDF1 dextro-looped transposition of the great arteries, congenital heart defects, multiple types, 6, dextro-looped transposition of the great arteries 3, dextro-looped transposition of the great arteries caused by mutation in GDF1, dextro-looped transposition of the great arteries type 3, transposition of the great arteries, dextro-looped 3, transposition of the great arteries, dextro-looped 3, formerly, transposition of the great arteries, dextro-looped type 3
congenital hereditary endothelial dystrophy of cornea
Also known as: CHED, CHED2, CHED2, formerly, CHEDII, autosomal recessive CHED, autosomal recessive congenital hereditary endothelial dystrophy, congenital hereditary endothelial dystrophy of cornea, congenital hereditary endothelial dystrophy of the cornea, congenital hereditary endothelial dystrophy type 2, congenital hereditary endothelial dystrophy type II, corneal dystrophy, congenital hereditary endothelial, corneal endothelial dystrophy, corneal endothelial dystrophy 2, corneal endothelial dystrophy 2, autosomal recessive, corneal endothelial dystrophy 2, autosomal recessive, formerly, corneal endothelial dystrophy type 2, corneal endothelial dystrophy, autosomal recessive, infantile hereditary endothelial dystrophy
congenital hereditary endothelial dystrophy type I
Also known as: CHED1, CHEDI, autosomal dominant CHED, autosomal dominant congenital hereditary endothelial dystrophy, congenital hereditary endothelial dystrophy type 1
congenital hereditary facial paralysis-variable hearing loss syndrome
Also known as: congenital hereditary facial palsy with variable deafness, congenital hereditary facial palsy with variable hearing loss, congenital hereditary facial paralysis with variable deafness, congenital hereditary facial paralysis-variable deafness syndrome
congenital herpes simplex virus infection
Also known as: Simplexvirus caused infectious embryofetopathy, Simplexvirus infectious embryofetopathy, antenatal herpes simplex virus infection, congenital herpes simplex, congenital herpes simplex infection, mother-to-child transmission of herpes simplex virus infection, neonatal HSV infection, neonatal herpes simplex, neonatal herpes simplex virus infection
Congenital high airway obstruction syndrome
Also known as: CHAOS