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
CED1 21093
Sensenbrenner syndrome 21093
Levin syndrome 1 21093
cranioectodermal dysplasia 1 21093
cranioectodermal dysplasia caused by mutation in IFT122 21093
cranioectodermal dysplasia 1; CED1 http://purl.obolibrary.org/obo/MONDO_0021093
IFT122 cranioectodermal dysplasia 21093
cranioectodermal dysplasia type 1 21093