MedGen Find_IDs Find_Terms Annotation
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created at 2024-09-19 07:43:07 UTC
updated at 2024-09-23 18:19:38 UTC
MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
622,528 entries

There is 0 pattern entry.

Label
Id
ARCMT2X C5569024
CMT2X C5569024
Charcot-Marie-Tooth neuropathy type 2X C5569024
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2X C5569024
Charcot-Marie-Tooth disease caused by mutation in SPG11 C5569024
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2X C5569024
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X C5569024
autosomal recessive Charcot Marie Tooth disease type 2X C5569024
Autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 (SPG11 vesicle trafficking associated, spatacsin) mutation C5569024
Autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 mutation C5569024
autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 mutation C5569024
Autosomal recessive Charcot-Marie-Tooth disease type 2X C5569024
autosomal recessive Charcot-Marie-Tooth disease type 2X C5569024
autosomal recessive axonal Charcot-Marie-Tooth disease type 2X C5569024
Charcot-Marie-Tooth disease axonal type 2X C5569024
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