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
susceptibility to atypical hemolytic uremic syndrome 6 13044
cortex disorder, auditory D001304
cortex disorders, auditory D001304
dysfunction, central auditory D001304
dysfunctions, central auditory D001304
familial cerebral cavernous malformation caused by mutation in CCM2 11304
CCM2 familial cerebral cavernous malformation 11304
spastic quadriplegic cerebral palsy 3 13048
auditory diseases, central D001304
auditory dysfunction, central D001304
lactate dehydrogenase deficiency type A 13047
enolase 3 deficiency 13046
muscle enolase deficiency 13046
muscular enolase deficiency 13046
LDH-M subunit deficiency 13047