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
congenital alopecia, and nail dystrophy t-cell immunodeficiency C536781
lymphoproliferative syndrome, ebv-associated, autosomal, 1 C567815
oligodactylous clubfeet, and anonychia-nail hypoplasia syndrome fibular agenesis-hypoplasia C567819
axillary neoplasm, benign 36781
primary, 3 biliary cirrhosis C567816
primary, 2 biliary cirrhosis C567817
Helicobacter pylori caused disease or disorder 6781
t-cell immunodeficiency, congenital alopecia, and nail dystrophy C536781
insulin-dependent, 24 diabetes mellitus C567818
Helicobacter pylori disease or disorder 6781
maternal 14q32.2 microdeletion syndrome 16781
juvenile spring eruption of ears C566781
toxoplasmosis, central nervous system D016781
benign axillary neoplasm 36781
fibular agenesis-hypoplasia, oligodactylous clubfeet, and anonychia-nail hypoplasia syndrome C567819