Visualize Submit Comment
Metadata
ID DOID:0111206
Name autosomal dominant distal hereditary motor neuronopathy 2
Definition An autosomal dominant distal hereditary motor neuronopathy that is characterized by onset of slowly progressive distal limb weakness and atrophy between the second and fifth decades of life.
https://www.ncbi.nlm.nih.gov/pubmed/15122253, https://www.ncbi.nlm.nih.gov/pubmed/1517763
Xrefs

MESH:C580044

OMIM:158590

ORDO:139525

UMLS_CUI:C3711384

Alternateids

DOID:0111208

Subsets

DO_rare_slim

Synonyms

autosomal dominant adult spinal muscular atrophy IIA [EXACT]

distal hereditary motor neuronopathy type 2 [EXACT]

distal hereditary motor neuronopathy type 2A [EXACT]

distal hereditary motor neuropathy type II [EXACT]

distal hereditary motor neuropathy type IIA [EXACT]

HMN II [EXACT]

HMN IIA [EXACT]

HMN2 [EXACT]

HMN2A [EXACT]

spinal Charcot-Marie-Tooth disease IIA [EXACT]

Parent Relationships

is_a autosomal dominant distal hereditary motor neuronopathy

Add an item to the term tracker