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:0111215 Direct  false
Redundant  false

1 Child Term

Identifier Name Description
DOID:0111215 autosomal dominant distal hereditary motor neuronopathy 8 An autosomal dominant distal hereditary motor neuronopathy that is characterized by congenital, non-progressive, predominantly distal, lower limb muscle weakness and atrophy with variable severity that has_material_basis_in heterozygous mutation in the TRPV4 gene on 12q24.11.

1 Parent Term

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