|
congenital prothrombin deficiency
|
13361 |
|
|
hereditary prothrombin deficiency
|
13361 |
|
|
neoplasms, sublingual gland
|
D013362 |
|
|
disease, submandibular gland
|
D013364 |
|
|
diseases, submandibular gland
|
D013364 |
|
|
neoplasm, submandibular gland
|
D013365 |
|
|
neoplasms, submandibular gland
|
D013365 |
|
|
cardiomyopathy, familial hypertrophic 7
|
13369 |
|
|
STX11 genetic hemophagocytic lymphohistiocytosis
|
11336 |
|
|
cardiomyopathy, familial hypertrophic, 7
|
13369 |
|
|
cardiomyopathy, familial hypertrophic, 7; CMH7
|
http://purl.obolibrary.org/obo/MONDO_0013369 |
|
|
cardiomyopathy, familial hypertrophic, type 7
|
13369 |
|
|
microcephaly, mental retardation, and distinctive facies, with Cardiac and genitourinary malformations
|
13362 |
|
