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
spherocytosis, hereditary, 4 12981
spherocytosis, type 4 12981
spherocytosis, type 4; SPH4 http://purl.obolibrary.org/obo/MONDO_0012981
hereditary spherocytosis 5 12985
spherocytosis, hereditary, 5 12985
spherocytosis, type 5 12985
agammaglobulinemia 6, autosomal recessive; AGM6 http://purl.obolibrary.org/obo/MONDO_0012987
spherocytosis, type 5; SPH5 http://purl.obolibrary.org/obo/MONDO_0012985
Kallmann syndrome 6 12988
CD79B autosomal agammaglobulinemia 12987
hereditary episodic ataxia caused by mutation in SLC1A3 12982
schizophrenia 8; SCZD8 http://purl.obolibrary.org/obo/MONDO_0011298
SLC1A3 hereditary episodic ataxia 12982
agammaglobulinemia 6, autosomal recessive 12987
stage 0 carcinoma of oropharynx 21298