|
seizures, benign familial infantile, type 3
|
11904 |
|
|
seizures, benign familial neonatal-infantile
|
11904 |
|
|
benign familial infantile epilepsy caused by mutation in SCN2A
|
11904 |
|
|
spirillum minus infection
|
D011906 |
|
|
streptobacillus moniliformis infection
|
D011906 |
|
|
syndrome, chromosome instability
|
21190 |
|
|
syndromes, chromosome instability
|
21190 |
|
|
autosomal dominant intermediate Charcot-Marie-Tooth disease type D
|
11909 |
|
|
juvenile myelomonocytic leukemia
|
11908 |
|
|
juvenile myelomonocytic leukemia; JMML
|
http://purl.obolibrary.org/obo/MONDO_0011908 |
|
|
infection, spirillum minus
|
D011906 |
|
|
infections, spirillum minus
|
D011906 |
|
|
endocarditides, streptobacillus moniliformis
|
D011906 |
|
|
endocarditis, streptobacillus moniliformis
|
D011906 |
|
|
infection, streptobacillus moniliformis
|
D011906 |
|
