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
milroy disease D008209
milroys disease D008209
nonne-milroy disease D008209
nonne-milroy lymphedema D008209
nonne-milroy-meige disease D008209
AxD type I 18209
hereditary lymphedema 1s D008209
CHAR syndrome; CHAR http://purl.obolibrary.org/obo/MONDO_0008209
patent ductus arteriosus with Facial Dysmorphism and abnormal fifth digits 8209
cerebral amyloid angiopathy, Itm2b-Related, 2 C538209
patent ductus arteriosus with facial dysmorphism and abnormal fifth digits 8209
dementia, familial danish C538209
hereditary lymphedema, congenital D008209
hereditary lymphedemas, congenital D008209
lymphedema, primary congenital D008209