Term Name:	obsolete distal hereditary motor neuronopathy type 7A
Synonyms:	DHMN7A, distal hereditary motor neuropathy type VIIA, distal spinal muscular atrophy with vocal cord paralysis type 7A, Harper-Young myopath, HMN VIIA, HMN7A
Definition:	A distal hereditary motor neuropathy type 7 characterized by slowly progressive distal atrophy and weakness affecting first the upper limbs and later the lower limbs and vocal cord paresis that has_material_basis_in heterozygous mutation in SLC5A7 on 2q12.3.
Ontology:	Human Disease [DOID:0111201]   ( DOID:0111201 )
Obsolete	true