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
spondylometaphyseal dysplasia, Algerian type 8478
hereditary optic Atrophies 43878
Mental Retardation, Autosomal Recessive 71 32789
esterase type B 7578
VWM syndrome, CACH D056784
classic 21-OHD CAH, salt wasting form 17839
classic 21-OHD CAH, simple virilizing form 17840
AML with CEBPA somatic mutations 17894
spondyloepiphyseal dysplasia, CHST3-Related C535789
vascular malformation, CNS D020785
vascular malformations, CNS D020785
venous angioma, CNS D020787
venous angiomas, CNS D020787
AIDS-related primary CNS lymphoma 6078
AIDS-Related primary CNS lymphoma http://purl.obolibrary.org/obo/MONDO_0006078