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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
3-methylglutaconic aciduria caused by mutation in OPA3 9787
immune-mediated protracted diarrhea of infancy 19787
Iraqi Jewish optic atrophy plus 9787
autosomal recessive optic atrophy plus syndrome 9787
autosomal recessive optic atrophy type 3 9787
optic atrophy plus syndrome 9787
Iraqi-Jewish 'optic atrophy plus 9787
Iraqi-Jewish optic atrophy plus 9787
Iraqi-Jewish 'optic atrophy plus' http://purl.obolibrary.org/obo/MONDO_0009787
Costeff optic atrophy syndrome 9787
infantile optic atrophy with chorea and spastic paraplegia 9787
severe immune-mediated enteropathy 19787
optic atrophy infantile with chorea and spastic paraplegia 9787
optic atrophy, infantile, with chorea and spastic paraplegia 9787
OPA3, autosomal recessive 9787