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