About   Help   FAQ
Disease Ontology Browser
autosomal dominant distal hereditary motor neuronopathy 1 (DOID:0111200)
Alliance: disease page
Synonyms: autosomal dominant distal juvenile spinal muscular atrophy type 1; dHMN1; distal hereditary motor neuronopathy type 1; distal hereditary motor neuropathy type I; HMN I; spinal Charcot-Marie-Tooth disease 1
Alt IDs: OMIM:182960, MESH:C566675, NCI:C132826, ORDO:139518, UMLS_CUI:C1866784
Definition: An autosomal dominant distal hereditary motor neuronopathy that is characterized by progressive distal motor weakness and muscular atrophy of the peripheral nervous system without sensory impairment, that is caused by anterior horn cell degeneration and that has_material_basis_in heterozygous 1.35-Mb DNA insertion on chromosome 7q34-q36.2. This structural variant (SV) results in the production of a novel gene-intergenic fusion transcript, UBE3C-IF.

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory