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
maculopathy, Impg2-related 13314
parotid carcinoma 21331
adrenal hyperplasia, congenital, due to cytochrome P450 oxidoreductase deficiency 13310
retinitis pigmentosa caused by mutation in ARL6 13312
retinitis pigmentosa caused by mutation in IMPG2 13314
retinitis pigmentosa caused by mutation in PDE6G 13315
maculopathy, Impg2-Related http://purl.obolibrary.org/obo/MONDO_0013314
retinitis pigmentosa 55 13312
retinitis pigmentosa 55; RP55 http://purl.obolibrary.org/obo/MONDO_0013312
retinitis pigmentosa 56 13314
retinitis pigmentosa 56; RP56 http://purl.obolibrary.org/obo/MONDO_0013314
retinitis pigmentosa 57 13315
retinitis pigmentosa 57; RP57 http://purl.obolibrary.org/obo/MONDO_0013315
parotid gland carcinoma 21331
injury, moral D013313