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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
chronic granulomatous disease caused by mutation in NCF1 9309
soluble oxidase component II, deficiency of 9309
late-onset junctional epidermolysis bullosa 19309
Ncf1, deficiency of 9309
NCF1 chronic granulomatous disease 9309
Soc2, deficiency of 9309
p47-PHOX, deficiency of 9309
CGD, autosomal recessive cytochrome B-positive, type 1 9309
acanthoma, pilar sheath D049309
acanthomas, pilar sheath D049309