Mondo_2019_Kim Find_IDs Find_Terms Annotation
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created at 2021-12-20 07:01:32 UTC
updated at 2021-12-22 01:40:39 UTC
Mondo_2019_Kim from bioportal
113,078 entries
Label
Id
ADOS http://purl.obolibrary.org/obo/MONDO_0007779
GBBB2 http://purl.obolibrary.org/obo/MONDO_0007779
BBB syndrome http://purl.obolibrary.org/obo/MONDO_0007779
G syndrome http://purl.obolibrary.org/obo/MONDO_0007779
GBBB syndrome http://purl.obolibrary.org/obo/MONDO_0007779
Opitz-Frias syndrome http://purl.obolibrary.org/obo/MONDO_0007779
hypertelorism-hypospadias syndrome http://purl.obolibrary.org/obo/MONDO_0007779
hypospadias-dysphagia syndrome http://purl.obolibrary.org/obo/MONDO_0007779
telecanthus-hypospadias syndrome http://purl.obolibrary.org/obo/MONDO_0007779
autosomal dominant Opitz BBB/G syndrome http://purl.obolibrary.org/obo/MONDO_0007779
autosomal dominant Opitz G/BBB syndrome http://purl.obolibrary.org/obo/MONDO_0007779
autosomal dominant Opitz syndrome http://purl.obolibrary.org/obo/MONDO_0007779
telecanthus with associated abnormalities http://purl.obolibrary.org/obo/MONDO_0007779
chromosome 22Q11.2 deletion syndrome, Opitz phenotype http://purl.obolibrary.org/obo/MONDO_0007779
hypertelorism with esophageal Abnormality and hypospadias http://purl.obolibrary.org/obo/MONDO_0007779