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
UV-sensitive syndrome caused by mutation in ERCC6 10909
Charcot-Marie-Tooth disease caused by mutation in MPZ 11909
glioblastoma, giant cell D005909
glioblastomas, giant cell D005909
diabetes mellitus complication D048909
diabetes mellitus complications D048909
diabetes related complications D048909
thyroglossal tract cyst C536909
Pituitary hormone deficiency, combined with rigid cervical spine 9091
arachnodactyly, and congenital contractures blepharophimosis C535909
glutathione synthetase deficiency 17909
specific antibody deficiency 19093
pituitary hormone deficiency, combined, 3 9091
leukoencephalopathy, hereditary diffuse, with spheroids 9096
leukoencephalopathy, hereditary diffuse, with spheroids; HDLS http://purl.obolibrary.org/obo/MONDO_0009096