MPZ

Deellabo: PGD DNA
Gen (Gen Code): MPZ
Aliases Gen: CHM, CMT1, CMT1B, CMT2I, CMT2J, CMT4E, CMTDI3, DSS, HMSNIB, MPP, P0
Gen ID (NCBI): 4359
OMIM Gen ID: 159440
Chromosomale locatie: 1q23.3
Genetische aandoening / Analyse: Charcot-Marie-Tooth, ziekte van, type 1B (CMT1B)
OMIM aandoening ID: 118200
Overerving: AD
Aliases aandoening: CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B 
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
PERONEAL MUSCULAR ATROPHY
CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL DOMINANT, WITH FOCALLY FOLDED MYELIN SHEATHS, TYPE 1B

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