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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
Hyper-IgE syndrome with atypical mycobacteriosis, autosomal recessive C566928
hypophysitides, idiopathic granulomatous D000069281
hypophysitis, idiopathic granulomatous D000069281
Anti-PIT-1 antibody syndromes D000069281
vitreoretinopathy, neovascular inflammatory 6928
vitreoretinopathy, neovascular inflammatory, autosomal dominant 6928
autosomal dominant neovascular inflammatory vitreoretinopathy 6928
partial duplication of chromosome type 7 16928
idiopathic granulomatous hypophysitides D000069281
IgG4 related hypophysitis D000069281
granulomatous hypophysitides, idiopathic D000069281
granulomatous hypophysitis, idiopathic D000069281
partial duplication of chromosome 7 16928
partial trisomy of chromosome 7 16928
Anti-PIT-1 antibody syndrome D000069281