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
pituitary dwarfism 3 9878
noonan syndrome 3 C537847
Oral-facial-digital syndrome 3 C557817
familial thoracic 3 aortic aneurysm C537783
posterior polymorphous, 3 corneal dystrophy C563788
fuchs endothelial, 3 corneal dystrophy C567678
optic atrophy 3, autosomal recessive 9787
deficiency of 3-beta-hydroxysteroid-delta(5)-desaturase C537880
spastic paraplegia 39, autosomal recessive 12787
synpolydactyly, 3, 3-prime, 4, associated with metacarpal and metatarsal synostoses C564278
spastic paraplegia 39 12787
spastic paraplegia 39, autosomal recessive; SPG39 http://purl.obolibrary.org/obo/MONDO_0012787
fibromatosis, gingival, 3; GINGF3 http://purl.obolibrary.org/obo/MONDO_0012378
Joubert syndrome 3; JBTS3 http://purl.obolibrary.org/obo/MONDO_0012078
mirror movements 3; MRMV3 http://purl.obolibrary.org/obo/MONDO_0014478