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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 (1)

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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last database update
08/03/2022
MGI 6.21
The Jackson Laboratory