Search Ontology:
Human Disease
Charcot-Marie-Tooth disease X-linked recessive 4
- Term ID
- DOID:0110212
- Synonyms
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- axonal motor sensory neuropathy with deafness and mental retardation
- Charcot-Marie-Tooth disease with deafness and mental retardation
- CMT4X
- CMTX4
- NADMR
- NAMSD
- X-linked Charcot-Marie-Tooth disease type 4
- Definition
- A Charcot-Marie-Tooth disease X-linked that has_material_basis_in mutation in the AIFM1 gene on chromosome Xq26. https://www.ncbi.nlm.nih.gov/pubmed/23217327
- References
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- ICD10CM:G60.0
- MIM:310490
- ORDO:101078
- Ontology
- Human Disease ( DOID:0110212 )
- is a type of
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Genes Involved
Zebrafish Models