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
CDD 21021
dominantly inherited craniodiaphyseal dysplasia 21021
Schaefer Stein Oshman syndrome 21021
craniodiaphyseal dysplasia, autosomal dominant 21021
craniodiaphyseal dysplasia, autosomal dominant; CDD http://purl.obolibrary.org/obo/MONDO_0021021
craniodiaphyseal dysplasia, dominant 21021