Familial hypertrophic cardiomyopathy

Part of

Sub-types of Familial hypertrophic cardiomyopathy

• Myotonic dystrophy type 1 45 trials
  1 sub-type

  • Congenital-onset Steinert myotonic dystrophy 1 trial
• Noonan syndrome and Noonan-related syndrome 1 trial · 29 incl. sub-types
  6 sub-types

  • Noonan syndrome 22 trials · 25 incl. sub-types Sub-types →
  • Costello syndrome 7 trials
  • Cardiofaciocutaneous syndrome 7 trials Sub-types →
  • Legius syndrome 5 trials
  • Noonan syndrome with multiple lentigines 3 trials Sub-types →
  • Noonan syndrome-like disorder with loose anagen hair 0 trials Sub-types →
• Beckwith-Wiedemann syndrome 6 trials
  8 sub-types

  • Beckwith-Wiedemann syndrome due to 11p15 microdeletion 0 trials
  • Beckwith-Wiedemann syndrome due to 11p15 microduplication 0 trials
  • Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion 0 trials
  • Beckwith-Wiedemann syndrome due to CDKN1C mutation 0 trials
  • Beckwith-Wiedemann syndrome due to NSD1 mutation 0 trials
  • Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 0 trials
  • Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 0 trials
  • Franceschini Vardeu Guala syndrome 0 trials
• Dilated cardiomyopathy 1C 1 trial
• Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency 1 trial
• Multiple acyl-CoA dehydrogenase deficiency 1 trial
  5 sub-types

  • Glutaric acidemia IIa 0 trials
  • Glutaric acidemia IIb 0 trials
  • Glutaric acidemia IIc 0 trials
  • Multiple acyl-CoA dehydrogenase deficiency, mild type 0 trials
  • Multiple acyl-CoA dehydrogenase deficiency, severe neonatal type 0 trials
• Very long chain acyl-CoA dehydrogenase deficiency 1 trial
• 46,XY complete gonadal dysgenesis 0 trials · 1 incl. sub-types
  12 sub-types

  • 46,XY sex reversal 5 1 trial
  • 46,XY disorder of sex development due to testicular 17,20-desmolase deficiency 0 trials
  • 46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome 0 trials
  • 46,XY sex reversal 1 0 trials
  • 46,XY sex reversal 10 0 trials
  • 46,XY sex reversal 11 0 trials
  • 46,XY sex reversal 2 0 trials
  • 46,XY sex reversal 3 0 trials
  • 46,XY sex reversal 4 0 trials
  • 46,XY sex reversal 6 0 trials
  • 46,XY sex reversal 7 0 trials
  • 46,XY sex reversal 9 0 trials
• Cardiomyopathy, familial hypertrophic 27 0 trials
• Cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction 0 trials
• Cardiomyopathy, familial hypertrophic, 28 0 trials
• Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies 0 trials
• Cardiomyopathy, familial hypertrophic, 30, atrial 0 trials
• Cardiomyopathy, familial hypertrophic, 31 0 trials
• Cardiomyopathy, familial restrictive, 5 0 trials
• Cardiomyopathy-hypotonia-lactic acidosis syndrome 0 trials
• Dilated cardiomyopathy 1KK 0 trials
• Hypertrophic cardiomyopathy 1 0 trials
• Hypertrophic cardiomyopathy 10 0 trials
• Hypertrophic cardiomyopathy 11 0 trials
• Hypertrophic cardiomyopathy 12 0 trials
• Hypertrophic cardiomyopathy 13 0 trials
• Hypertrophic cardiomyopathy 14 0 trials
• Hypertrophic cardiomyopathy 15 0 trials
• Hypertrophic cardiomyopathy 16 0 trials
• Hypertrophic cardiomyopathy 17 0 trials
• Hypertrophic cardiomyopathy 18 0 trials
• Hypertrophic cardiomyopathy 19 0 trials
• Hypertrophic cardiomyopathy 2 0 trials
• Hypertrophic cardiomyopathy 20 0 trials
• Hypertrophic cardiomyopathy 21 0 trials
• Hypertrophic cardiomyopathy 25 0 trials
• Hypertrophic cardiomyopathy 26 0 trials
• Hypertrophic cardiomyopathy 3 0 trials
• Hypertrophic cardiomyopathy 4 0 trials
• Hypertrophic cardiomyopathy 6 0 trials
• Hypertrophic cardiomyopathy 7 0 trials
• Hypertrophic cardiomyopathy 8 0 trials
• Hypertrophic cardiomyopathy 9 0 trials
• Long chain acyl-CoA dehydrogenase deficiency 0 trials