MONDO_merge Find_IDs Find_Terms Annotation
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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
neuropathy, hereditary sensory and autonomic, type 2B 13142
neuropathy, hereditary sensory and autonomic, type IIB 13142
neuropathy, hereditary sensory and autonomic, type IIB; HSAN2B http://purl.obolibrary.org/obo/MONDO_0013142
KCNE3 Brugada syndrome 13145
SCN3B Brugada syndrome 13146
HCN4 Brugada syndrome 13148
dilated cardiomyopathy type 1CC 13147
cardiomyopathy, dilated, type 1Cc 13147
candidiasis, familial, type 4 13140
Graves disease, susceptibility to, 2 11314
Graves disease, susceptibility to, type 2 11314
thrombophilia due to antithrombin 3 deficiency 13144
thrombophilia due to antithrombin III deficiency 13144
thrombophilia due to elevated histidine-rich glycoprotein 13143
thrombophilia due to histidine-rich glycoprotein deficiency 13143