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Disease Ontology Browser
Charcot-Marie-Tooth disease type 4D (DOID:0110186)
Synonyms: autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4D; Charcot-Marie-Tooth neuropathy type 4D; CMT4D; hereditary motor abd sensory neuropathy LOM type; HMSN4D; HMSN Lom type; HMSN-Lom; HMSNL
Alt IDs: OMIM:601455, ICD10CM:G60.0, ORDO:99950
Definition: A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the N-myc downstream-regulated gene-1 (NDRG1) on chromosome 8q24.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/11/2017
MGI 6.10
The Jackson Laboratory