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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
thalamic syndrome D013786
thalamic syndromes D013786
cone-ROD dystrophy 16; CORD16 http://purl.obolibrary.org/obo/MONDO_0013786
hyperthyroidism, congenital nonautoimmune C563786
cone-rod dystrophy caused by mutation in C8orf37 13786
C8orf37 cone-rod dystrophy 13786
ocular, type i albinism C537863
laplane fontaine lagardere syndrome C537869
x-linked cutis laxa C537860
hyperthyroidism, nonautoimmune, autosomal dominant C563786
serous membrane inflammation 43786
nonautoimmune, autosomal dominant hyperthyroidism C563786
retinitis pigmentosa 64 13786
childhood testicular choriocarcinoma 3786
pediatric testicular choriocarcinoma 3786