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
ARCMT2X 14726
CMT2X 14726
autosomal recessive axonal Charcot-Marie-Tooth disease type 2X 14726
autosomal recessive Charcot Marie Tooth disease type 2X 14726
autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 mutation 14726
autosomal recessive Charcot-Marie-Tooth disease type 2X 14726
Charcot-Marie-Tooth disease axonal type 2X 14726
Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2X 14726
Charcot-Marie-Tooth disease, axonal, type 2X 14726
Charcot-Marie-Tooth disease, axonal, type 2X; CMT2X http://purl.obolibrary.org/obo/MONDO_0014726
Charcot-Marie-Tooth disease, axonal, type 2x 14726
Charcot-Marie-Tooth neuropathy type 2X 14726
Charcot-Marie-Tooth disease caused by mutation in SPG11 14726
SPG11 Charcot-Marie-Tooth disease 14726
Charcot-Marie-Tooth neuropathy, type 2X 14726