| KMT2B |
Dystonia |
phenotype |
Sign or Symptom |
0.31 |
DisGeNET |
| KMT2B |
Dystonia, Paroxysmal |
phenotype |
Sign or Symptom |
0.30 |
DisGeNET |
| KMT2B |
Dystonia Disorders |
group |
Disease or Syndrome |
0.31 |
DisGeNET |
| KMT2B |
Idiopathic familial dystonia |
disease |
Disease or Syndrome |
0.30 |
DisGeNET |
| KMT2B |
Dystonia, Diurnal |
phenotype |
Sign or Symptom |
0.30 |
DisGeNET |
| KMT2B |
Focal Dystonia |
disease |
Disease or Syndrome |
0.30 |
DisGeNET |
| KMT2B |
Dystonia, Limb |
phenotype |
Sign or Symptom |
0.30 |
DisGeNET |
| KMT2B |
Adult-Onset Dystonias |
disease |
Disease or Syndrome |
0.30 |
DisGeNET |
| KMT2B |
Adult-Onset Idiopathic Focal Dystonias |
disease |
Disease or Syndrome |
0.30 |
DisGeNET |
| KMT2B |
Adult-Onset Idiopathic Torsion Dystonias |
disease |
Disease or Syndrome |
0.30 |
DisGeNET |
| KMT2B |
Autosomal Dominant Familial Dystonia |
disease |
Disease or Syndrome |
0.30 |
DisGeNET |
| KMT2B |
Autosomal Recessive Familial Dystonia |
disease |
Disease or Syndrome |
0.30 |
DisGeNET |
| KMT2B |
Childhood Onset Dystonias |
disease |
Disease or Syndrome |
0.30 |
DisGeNET |
| KMT2B |
Dystonia, Primary |
disease |
Disease or Syndrome |
0.30 |
DisGeNET |
| KMT2B |
Dystonia, Secondary |
disease |
Disease or Syndrome |
0.30 |
DisGeNET |
| KMT2B |
Dystonias, Sporadic |
disease |
Disease or Syndrome |
0.30 |
DisGeNET |
| KMT2B |
Familial Dystonia |
disease |
Disease or Syndrome |
0.30 |
DisGeNET |
| KMT2B |
Pseudodystonia |
disease |
Mental or Behavioral Dysfunction |
0.30 |
DisGeNET |
| KMT2B |
Liver carcinoma |
disease |
Neoplastic Process |
0.36 |
DisGeNET |
| KMT2B |
Intellectual Disability |
group |
Mental or Behavioral Dysfunction |
0.32 |
DisGeNET |
| KMT2B |
DYSTONIA 28, CHILDHOOD-ONSET |
disease |
Disease or Syndrome |
0.40 |
DisGeNET |
| KMT2B |
Writer's Cramp |
disease |
Disease or Syndrome |
0.30 |
DisGeNET |