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
CMT2W 14711
autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS mutation 14711
autosomal dominant Charcot-Marie-Tooth disease type 2W 14711
autosomal dominant axonal Charcot-Marie-Tooth disease type 2W 14711
Charcot-Marie-Tooth disease, axonal type 2W 14711
Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2W 14711
Charcot-Marie-Tooth disease, axonal, type 2W 14711
Charcot-Marie-Tooth disease, axonal, type 2W; CMT2W http://purl.obolibrary.org/obo/MONDO_0014711
Charcot-Marie-Tooth disease, axonal, type 2w 14711
HARS Charcot-Marie-Tooth disease type 2 14711
Charcot-Marie-Tooth disease type 2 caused by mutation in HARS 14711
Charcot-Marie-Tooth neuropathy type 2W 14711
Charcot-Marie-Tooth neuropathy, type 2W 14711