Additional Disease Briefs

cardiomyopathy, familial hypertrophic 27

Also known as: CMH27, cardiomyopathy, FAMILIAL hypertrophic 27

cardiomyopathy, familial hypertrophic, 28

Also known as: CMH28, cardiomyopathy, familial hypertrophic, 28

cardiomyopathy, familial restrictive, 1

cardiomyopathy, familial restrictive, 2

Also known as: RCM2, cardiomyopathy, familial restrictive, 2

cardiomyopathy, familial restrictive, 3

Also known as: RCM3, TNNT2 familial isolated restrictive cardiomyopathy, cardiomyopathy, familial restrictive, 3, cardiomyopathy, familial restrictive, type 3, familial isolated restrictive cardiomyopathy caused by mutation in TNNT2

cardiomyopathy, familial restrictive, 6

Also known as: RCM6, cardiomyopathy, familial restrictive, 6

cardiospondylocarpofacial syndrome

Also known as: CSCF, Forney Robinson Pascoe syndrome, Forney syndrome, Forney-Robinson-Pascoe syndrome, cardiospondylocarpofacial syndrome, congenital heart disease, deafness, and skeletal malformations, mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones, mitral regurgitation-deafness-skeletal anomalies syndrome

Carney complex

Also known as: CNC, Carney Complex, type 1, Carney Complex, type 2, Carney complex, Carney syndrome, Carney's syndrome, LAMB, Myxoma - spotty pigmentation - endocrine overactivity, Myxoma-spotty pigmentation-endocrine overactivity syndrome, NAME syndrome, atrial myxoma with lentigines, lamb, lamb syndrome, lentigines, atrial myxoma, mucocutaneous myoma, blue Nevus syndrome, nevi, atrial myxoma, skin myxoma, ephelides syndrome

Carney complex – trismus – pseudocamptodactyly syndrome

Also known as: CARNEY complex variant, Carney complex variantCARNEY complex variant, Carney complex variant

Carney complex – trismus – pseudocamptodactyly syndrome

Also known as: CARNEY complex variant, Carney complex variant