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
spastic paraplegia 50, autosomal recessive; SPG50 http://purl.obolibrary.org/obo/MONDO_0013048
D-HUS with I factor anomaly 13041
D-HUS with B factor anomaly 13042
aHUS with B factor anomaly 13042
D-HUS with C3 anomaly 13043
aHUS with C3 anomaly 13043
lactate dehydrogenase A deficiency 13047
aHUS with I factor anomaly 13041
CCM2 familial cerebral cavernous malformation 11304
susceptibility to atypical hemolytic uremic syndrome 2 13040
susceptibility to atypical hemolytic uremic syndrome 3 13041
susceptibility to atypical hemolytic uremic syndrome 4 13042
susceptibility to atypical hemolytic uremic syndrome 5 13043
susceptibility to atypical hemolytic uremic syndrome 6 13044
cortex disorder, auditory D001304