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
deficiency, potassium D011191
potassium deficiencies D011191
hypotrichosis-lymphedema-telangiectasia syndrome; HLTS http://purl.obolibrary.org/obo/MONDO_0011914
autosomal recessive axonal CMT4C4 11916
autosomal recessive axonal Charcot-Marie-Tooth disease disease type 2K 11916
autosomal recessive axonal Charcot-Marie-Tooth disease type 2K 11916
Charcot-Marie-Tooth disease axonal type 2K 11916
Charcot-Marie-Tooth neuropathy axonal type 2K 11916
Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2K 11916
Charcot-Marie-Tooth disease, axonal, type 2K 11916
Charcot-Marie-Tooth neuropathy, axonal, type 2K 11916
Charcot-Marie-Tooth disease, axonal, type 2K; CMT2K http://purl.obolibrary.org/obo/MONDO_0011916
Hirudinea caused disease or disorder 1191
Hirudinea infectious disease 1191
familial Alzheimer disease, type 3 11913