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
CMT1B 7307
HMSN1 7307
HMSN1B 7307
Hmsn1 http://purl.obolibrary.org/obo/MONDO_0007307
Hmsn1B http://purl.obolibrary.org/obo/MONDO_0007307
CMT 1B 7307
HMSN 1B 7307
HMSN IB 7307
c6 deficiency C567307
hereditary motor and sensory neuropathy 1 7307
autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B 7307
Charcot Marie Tooth disease type 1B 7307
hereditary motor and sensory neuropathy 1B 7307
hereditary motor and sensory neuropathy IB 7307
Charcot-Marie-Tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1B 7307