Krankheit

Neuropathie (hereditär motorisch-sensorisch) Typ 1B

CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B

OMIM: 118200

Synonyme

  • HMSN1
  • CMT1B
  • Charcot-Marie-Tooth-Krankheit Typ 1B
  • HEREDITARY MOTOR AND SENSORY NEUROPATHY I; HMSN I
  • HEREDITARY MOTOR AND SENSORY NEUROPATHY IB; HMSN IB
  • HMSN1
  • HMSN1B
  • CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 1B
  • CHARCOT-MARIE-TOOTH DISEASE, SLOW NERVE CONDUCTION TYPE, LINKED TO DUFFY
  • CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B
  • PERONEAL MUSCULAR ATROPHY
  • CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL DOMINANT, WITH FOCALLY FOLDED MYELIN SHEATHS, TYPE 1B

Gen locations