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
retinal cone dystrophy 3A; RCD3A http://purl.obolibrary.org/obo/MONDO_0012398
retinal cone dystrophy type 3A 12398
NCL, Northern epilepsy variant 12391
hyperinsulinemic hypoglycemia familial 7 12396
hyperinsulinemic hypoglycemia exercise-induced 12396
hyperinsulinemic hypoglycemia, exercise-induced 12396
complex cortical dysplasia with other brain malformations 7 12399
complex cortical dysplasia with other brain malformations caused by mutation in TUBB2B 12399
complex cortical dysplasia with other brain malformations type 7 12399
hyperinsulinemic hypoglycemia, familial, 7 12396
hyperinsulinemic hypoglycemia, familial, 7; HHF7 http://purl.obolibrary.org/obo/MONDO_0012396
hyperinsulinemic hypoglycemia, familial, type 7 12396
CLN8 disease, late infantile (subtype) 12391
exercise induced hyperinsulinemic hypoglycemia 12396
exercise-induced hyperinsulinemic hypoglycemia 12396