MONDO_merge Find_IDs Find_Terms Annotation
manager
language -
license -
created at 2021-12-22 03:08:20 UTC
updated at 2021-12-22 07:06:09 UTC
MONDO_bioport_pref_name
183,974 entries
Label
Id
hyperphenylalaninemia due to DNAJC12 deficiency 44304
LDHA glycogen storage disease 13047
mycobacterium tuberculosis, susceptibility to, 3 13045.0
Graves disease, susceptibility to, X-linked 1 10304
Graves disease, susceptibility to, X-linked 2 10304
Graves disease, susceptibility to, X-linked type 1 10304
atypical hemolytic-uremic syndrome with B factor anomaly 13042
atypical hemolytic-uremic syndrome with C3 anomaly 13043
atypical hemolytic-uremic syndrome with I factor anomaly 13041
atypical hemolytic-uremic syndrome with MCP/CD46 anomaly 13040
atypical hemolytic-uremic syndrome with thrombomodulin anomaly 13044
hemolytic uremic syndrome, atypical, susceptibility to, 2 13040
hemolytic uremic syndrome, atypical, susceptibility to, 2; AHUS2 http://purl.obolibrary.org/obo/MONDO_0013040
hemolytic uremic syndrome, atypical, susceptibility to, 3 13041
hemolytic uremic syndrome, atypical, susceptibility to, 3; AHUS3 http://purl.obolibrary.org/obo/MONDO_0013041