MONDO_merge (183,974) Find_IDs 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
Label
Id
CEP 9902
Cep 9902
Del(13)(q34) 19902
neuropapillitides D009902
neuropapillitis D009902
monosomy 13q34 19902
Gunther disease 9902
Günther disease 9902
Uros deficiency 9902
congenital porphyria 9902
cutaneous porphyria 9902
erythropoietic porphyria 9902
neuritides, optic D009902
neuritides, retrobulbar D009902
neuritis, optic D009902