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
congenital alopecia, and nail dystrophy t-cell immunodeficiency C536781
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
lymphoproliferative syndrome, ebv-associated, autosomal, 1 C567815
juvenile spring eruption of ears C566781
maternal 14q32.2 microdeletion syndrome 16781
benign axillary neoplasm 36781
toxoplasmosis, central nervous system D016781
fibular agenesis-hypoplasia, oligodactylous clubfeet, and anonychia-nail hypoplasia syndrome C567819