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DO Term : autosomal dominant distal hereditary motor neuronopathy 13 [DOID:0081401] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  An autosomal dominant distal hereditary motor neuronopathy that is characterized by distal muscle weakness and atrophy affecting both the upper and lower limbs, resulting in difficulty walking and poor fine hand motor skills and that has_material_basis_in heterozygous mutation in the BSCL2 gene on chromosome 11q12.
  • synonyms:
  • 619112,
  • OMIM:619112
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents