|
cardiomyopathy, congestive
|
7269 |
|
|
cardiomyopathy, dilated, 1A
|
7269 |
|
|
dilated cardiomyopathy 1A
|
7269 |
|
|
cardiomyopathy, dilated, 1A; CMD1A
|
http://purl.obolibrary.org/obo/MONDO_0007269 |
|
|
conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones mitral regurgitation
|
C537269 |
|
|
deafness, and skeletal malformations congenital heart disease
|
C537269 |
|
|
X-linked inherited ichthyosis syndromic form
|
17269 |
|
|
cardiomyopathy, familial idiopathic
|
7269 |
|
|
familial dilated cardiomyopathy with conduction defect due to LMNA mutation
|
7269 |
|
|
cardiomyopathy, idiopathic dilated
|
7269 |
|
|
familial isolated dilated cardiomyopathy caused by mutation in LMNA
|
7269 |
|
|
LMNA familial isolated dilated cardiomyopathy
|
7269 |
|
|
forney robinson pascoe syndrome
|
C537269 |
|
|
X-linked ichthyosis syndrome
|
17269 |
|
