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Disease Ontology Browser
Charcot-Marie-Tooth disease type 4D (DOID:0110186)
Alliance: disease page
Synonyms: autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4D; Charcot-Marie-Tooth neuropathy type 4D; CMT4D; hereditary motor and 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 (2)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory