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
CMT2V 14665
NAGLU Charcot-Marie-Tooth disease 14665
autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation 14665
autosomal dominant Charcot-Marie-Tooth disease type 2V 14665
autosomal dominant axonal Charcot-Marie-Tooth disease type 2V 14665
Charcot-Marie-Tooth disease axonal type 2V 14665
Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2V 14665
Charcot-Marie-Tooth disease, axonal, type 2V 14665
Charcot-Marie-Tooth disease, axonal, type 2V; CMT2V http://purl.obolibrary.org/obo/MONDO_0014665
Charcot-Marie-Tooth disease caused by mutation in NAGLU 14665
hereditary adult-onset painful axonal polyneuropathy 14665
Charcot-Marie-Tooth neuropathy type 2V 14665
Charcot-Marie-Tooth neuropathy, type 2V 14665