MONDO_merge Find_IDs Find_Terms Annotation
manager
language -
license -
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
FGLDS1 8115
FS1 8115
Mmt syndrome 8115
Oded syndrome 8115
oculodigitoesophagoduodenal syndrome 8115
microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1 8115
microcephaly and digital abnormalities with Normal intelligence http://purl.obolibrary.org/obo/MONDO_0008115
microcephaly and digital abnormalities with normal intelligence 8115
microcephaly, intellectual disability, and tracheoesophageal fistula syndrome 8115
Feingold syndrome 1; FGLDS1 http://purl.obolibrary.org/obo/MONDO_0008115
Feingold syndrome caused by mutation in MYCN 8115
Feingold syndrome 1 8115
MMT type 1 8115
microcephaly-digital anomalies-normal intelligence syndrome type 1 8115
pigmentary abnormality of the anterior segment of the eye C538115