WormBase Tree Display for DO_term: DOID:3635

DOID:3635 Name: congenital myasthenic syndrome
  Status: Valid
  Definition: A neuromuscular junction disease that is characterized by weakness and easy fatiguability resulting from a genetic defect at the junction where the nerve stimulates muscle activity that result in muscle weakness and may affect nerve cells (presynaptic), muscle cells (postsynaptic) or the space between nerve and muscle cells (synaptic).
  Comment: Xref MGI.
  Parent: Is_a: DOID:439
      DOID:0080015
  Child: Is: DOID:0080587
      DOID:0110657
      DOID:0110658
      DOID:0110659
      DOID:0110660
      DOID:0110661
      DOID:0110662
      DOID:0110663
      DOID:0110664
      DOID:0110665
      DOID:0110666
      DOID:0110667
      DOID:0110668
      DOID:0110669
      DOID:0110670
      DOID:0110671
      DOID:0110672
      DOID:0110673
      DOID:0110674
      DOID:0110675
      DOID:0110676
      DOID:0110677
      DOID:0110678
      DOID:0110679
      DOID:0110680
      DOID:0110681
      DOID:0110682
      DOID:0110683
  Disease_model_annotation: WBDOannot00000869
    WBDOannot00000870
    WBDOannot00000871
    WBDOannot00000872
    WBDOannot00000873
    WBDOannot00000874
    WBDOannot00000875
  Attribute_of: Gene_by_biology: WBGene00006797
    Gene_by_orthology: WBGene00000047
      WBGene00002040
      WBGene00004897
      WBGene00004898
      WBGene00004921
      WBGene00004923
      WBGene00006797
      WBGene00010780
      WBGene00021345
    Disease_model_variation: WBVar00275227
      WBVar00275220
    Chemical_inducer: WBMol:00004019
      WBMol:00004765
    Molecule_modifier: WBMol:00001251
      WBMol:00003999