WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:231
Child Term . Identifier  DOID:0051042 Direct  false
Redundant  false

1 Child Term

Identifier Name Description
DOID:0051042 autosomal dominant distal hereditary motor neuronopathy 15 An autosomal dominant distal hereditary motor neuronopathy that is characterized by adult onset of slowly progressive distal weakness and atrophy of the lower limbs associated with absent reflexes and that has_material_basis_in heterozygous mutation in the BAG3 gene on chromosome 10q26.

1 Parent Term

Identifier Name Description
DOID:231 motor neuron disease A neurodegenerative disease that is located_in the motor neurons.