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
benign hypertensive renal disease 1304
cerebral palsy, spastic quadriplegic, 3, formerly 13048
hereditary spastic paraplegia 50 13048
hereditary spastic paraplegia caused by mutation in AP4M1 13048
hereditary spastic paraplegia type 50 13048
central auditory pathway disorders D001304
AP4M1 hereditary spastic paraplegia 13048
autosomal recessive spastic paraplegia 50 13048
mycobacterium tuberculosis, susceptibility to, 3 13045.0
atypical hemolytic-uremic syndrome with B factor anomaly 13042
atypical hemolytic-uremic syndrome with C3 anomaly 13043
atypical hemolytic-uremic syndrome with I factor anomaly 13041
atypical hemolytic-uremic syndrome with MCP/CD46 anomaly 13040
atypical hemolytic-uremic syndrome with thrombomodulin anomaly 13044
hemolytic uremic syndrome, atypical, susceptibility to, 2 13040