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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
autosomal dominant 38 deafness C563421
mixed cell adenoma 3421
hand-arm vibration syndrome D053421
classic complement early component deficiency caused by mutation in C8B 13421
vibration syndrome, hand-arm D053421
vibration syndromes, hand-arm D053421
resistance to thyroid hormone alpha 34216
hand-arm vibration syndromes D053421
resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha 34216
resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta 34217
C8 deficiency, type 2 13421
syndrome, hand-arm vibration D053421
syndromes, hand-arm vibration D053421
hand arm vibration syndrome D053421
C8 deficiency type II 13421