MONDO_merge Find_IDs Find_Terms Annotation
manager
language -
license -
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
spherocytosis, type 4; SPH4 http://purl.obolibrary.org/obo/MONDO_0012981
hereditary spherocytosis 5 12985
spherocytosis, hereditary, 5 12985
spherocytosis, type 5 12985
spherocytosis, type 5; SPH5 http://purl.obolibrary.org/obo/MONDO_0012985
Kallmann syndrome 6 12988
hypogonadotropic hypogonadism 6 with or without anosmia 12988
hypogonadotropic hypogonadism 6 with or without anosmia; HH6 http://purl.obolibrary.org/obo/MONDO_0012988
schizophrenia 8; SCZD8 http://purl.obolibrary.org/obo/MONDO_0011298
agammaglobulinemia 6, autosomal recessive 12987
CD79B autosomal agammaglobulinemia 12987
hereditary episodic ataxia caused by mutation in SLC1A3 12982
stage 0 carcinoma of oropharynx 21298
agammaglobulinemia 6, autosomal recessive; AGM6 http://purl.obolibrary.org/obo/MONDO_0012987
stage 0 carcinoma of the oropharynx 21298