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Diseases

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2F

autosomal dominant charcot-marie-tooth disease type 2f

Entity Type
Diseases
Relation Groups
1
Relation Preview
1

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2F
Standard Disease Name
autosomal dominant charcot-marie-tooth disease type 2f
MeSH Tree
No data
ICD-10
G60.0

Identifiers

DO ID
No data
MeSH ID
C535413
OMIM ID
606595
UMLS ID
C1847823
HPO ID
No data

Description and Extensions

Description
Autosomal dominant Charcot-Marie-Tooth disease type 2F (CMT2F) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. CMT2F is characterized by symmetric weakness prima
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease1 Targets
01
HSPB1
heat shock protein family B (small) member 1
heat shock protein family B (small) member 1