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Human Disease

Charcot-Marie-Tooth disease dominant intermediate G

Term ID
DOID:0080294
Synonyms
Definition
A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in heterozygous mutation in the NEFL gene on chromosome 8p21. https://pubmed.ncbi.nlm.nih.gov/28364294/
References
Ontology
Human Disease   ( DOID:0080294 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models