Mondo_2019_Kim Find_IDs Find_Terms Annotation
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created at 2021-12-20 07:01:32 UTC
updated at 2021-12-22 01:40:39 UTC
Mondo_2019_Kim from bioportal
113,078 entries

There is 0 pattern entry.

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