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
BFNS2 7366
SDHx-related paraganglioma-pheochromocytoma 17366
familial pheochromocytoma-paraganglioma 17366
hereditary paraganglioma-pheochromocytoma 17366
hereditary pheochromocytoma-paraganglioma 17366
neu deficiency C537366
neu1 deficiency C537366
neug deficiency C537366
sialidoses, type 2 C537366
KCNQ3 benign neonatal seizures 7366
sialidosis, type i C537366
convulsions, benign familial neonatal, 2 7366
seizures, benign familial neonatal, 2 7366
seizures, benign familial neonatal, 2; BFNS2 http://purl.obolibrary.org/obo/MONDO_0007366
seizures, benign familial neonatal, type 2 7366