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
posterior optic neuritis D009902
hereditary lichen planus 7902
partial deletion of the long arm of chromosome 3 16902
partial monosomy of the long arm of chromosome 3 16902
autosomal recessive osteopetrosis 19026
infantile malignant osteopetrosis 19026
autosomal recessive osteopetrosis (disease) 19026
optic neuritides, posterior D009902
optic neuritis, posterior D009902
glaucoma, secondary open angle D005902
chronic primary open angle glaucoma D005902
neuritis, anterior optic D009902
neuritides, anterior optic D009902
neuritides, posterior optic D009902
neuritis, posterior optic D009902