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
KCNQ2-related neonatal epileptic encephalopathy 13387
early infantile epileptic encephalopathy 12 13389
early infantile epileptic encephalopathy caused by mutation in PLCB1 13389
early infantile epileptic encephalopathy caused by mutation in SCN2A 13388
developmental and epileptic encephalopathy, 11 13388
developmental and epileptic encephalopathy, 12 13389
developmental and epileptic encephalopathy, 7 13387
recurrent vertigo, episodic D020338
recurrent vertigos, episodic D020338
vestibular nerve inflammation D020338
disease of eyelid 3382
disorder of eyelid 3382
primary ovarian failure arising through autoimmunity 44338
epilepsy, idiopathic generalized, susceptibility to, 4 12338
epilepsy, idiopathic generalized, susceptibility to, 4; EIG4 http://purl.obolibrary.org/obo/MONDO_0012338