|
self-improving collodion baby
|
17267 |
|
|
hypertrophic cardiomyopathy caused by mutation in TPM1
|
7267 |
|
|
langer mesomelic dwarfism
|
C537267 |
|
|
self-improving congenital ichthyosis
|
17267 |
|
|
TPM1 hypertrophic cardiomyopathy
|
7267 |
|
|
langer mesomelic dyspalsia
|
C537267 |
|
|
langer mesomelic dysplasia
|
C537267 |
|
|
cardiomyopathy familial hypertrophic 3
|
7267 |
|
|
cardiomyopathy, familial hypertrophic, 3
|
7267 |
|
|
cardiomyopathy, familial hypertrophic, 3; CMH3
|
http://purl.obolibrary.org/obo/MONDO_0007267 |
|
|
cardiomyopathy, familial hypertrophic, type 3
|
7267 |
|
|
fibula, and mandible type mesomelic dwarfism of the hypoplastic ulna
|
C537267 |
|
|
niemann-pick disease, intermediate, with visceral involvement and rapid progression
|
C567267 |
|
|
hypertrophic cardiomyopathy type 3
|
7267 |
|
|
langer type of mesomelic dwarfism
|
C537267 |
|
