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
partial deletion of chromosome 9q 16908
partial monosomy of chromosome 9q 16908
meningioma (disease) of clivus of occipital bone 3908
congenital disorder of glycosylation type 2a 8908
congenital disorder of glycosylation type IIa 8908
congenital disorder of glycosylation, type IIa 8908
congenital disorder of glycosylation, type IIa; CDG2A http://purl.obolibrary.org/obo/MONDO_0008908
partial monosomy of the long arm of chromosome 9 16908
thyrotoxic periodic paralysis, susceptibility to, 3 13908
thyrotoxic periodic paralysis, susceptibility to, 3; TTPP3 http://purl.obolibrary.org/obo/MONDO_0013908
Old Age pemphigus 19082
smith lemli opitz syndrome D019082
smith lemli opitz syndrome, type 1 D019082
smith lemli opitz syndrome, type 2 D019082
smith lemli opitz syndrome, type II D019082