DOID:0110170
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Charcot-Marie-Tooth disease axonal type 2Q
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Aliases:
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CMT2Q
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Charcot-Marie-Tooth neuropathy type 2Q
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autosomal dominant Charcot-Marie-Tooth disease type 2Q
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autosomal dominant axonal Charcot-Marie-Tooth disease type 2Q
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Mus musculus (house mouse)
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DOID:0110170
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Charcot-Marie-Tooth disease axonal type 2Q
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Aliases:
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CMT2Q
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Charcot-Marie-Tooth neuropathy type 2Q
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autosomal dominant Charcot-Marie-Tooth disease type 2Q
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autosomal dominant axonal Charcot-Marie-Tooth disease type 2Q
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Danio rerio (zebrafish)
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DOID:0110170
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Charcot-Marie-Tooth disease axonal type 2Q
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Aliases:
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CMT2Q
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Charcot-Marie-Tooth neuropathy type 2Q
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autosomal dominant Charcot-Marie-Tooth disease type 2Q
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autosomal dominant axonal Charcot-Marie-Tooth disease type 2Q
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Caenorhabditis elegans
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DOID:0110170
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Charcot-Marie-Tooth disease axonal type 2Q
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Aliases:
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CMT2Q
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Charcot-Marie-Tooth neuropathy type 2Q
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autosomal dominant Charcot-Marie-Tooth disease type 2Q
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autosomal dominant axonal Charcot-Marie-Tooth disease type 2Q
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Rattus norvegicus (Norway rat)
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DOID:0110169
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Charcot-Marie-Tooth disease axonal type 2P
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Aliases:
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CMT2P
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Charcot-Marie-Tooth disease type 2P
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Charcot-Marie-Tooth neuropathy type 2P
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Homo sapiens (human)
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DOID:0110168
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Charcot-Marie-Tooth disease type 2Y
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Aliases:
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CMT2 due to VCP mutation
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CMT2Y
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Charcot-Marie-Tooth neuropathy type 2Y
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autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation
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autosomal dominant axonal Charcot-Marie-Tooth type 2Y
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Homo sapiens (human)
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DOID:0110167
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Charcot-Marie-Tooth disease axonal type 2K
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Aliases:
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ARCMT2K
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Charcot-Marie-Tooth neuropathy axonal type 2K
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autosomal recessive Charcot-Marie-Tooth disease with hoarseness
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autosomal recessive axonal CMT4C4
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autosomal recessive axonal Charcot-Marie-Tooth disease disease type 2K
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autosomal recessive axonal Charcot-Marie-Tooth disease type 2K
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Homo sapiens (human)
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DOID:0110166
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Charcot-Marie-Tooth disease axonal type 2H
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Aliases:
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AR-CMT2C
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Autosomal recessive axonal CMT4C2
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Axonal Charcot-Marie-Tooth disease with pyramidal involvement
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CMT2H
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Charcot-Marie-Tooth disease type 2H
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autosomal recessive axonal Charcot-Marie-Tooth disease with pyramidal features
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autosomal recessive axonal Charcot-Marie-Tooth neuropathy with pyramidal features
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Homo sapiens (human)
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DOID:0110165
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Charcot-Marie-Tooth disease type 2E
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Aliases:
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CMT2E
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Charcot-Marie-Tooth neuropathy type 2E
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autosomal dominant Charcot-Marie-Tooth disease type 2E
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Homo sapiens (human)
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DOID:0110164
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Charcot-Marie-Tooth disease type 2D
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Aliases:
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CMT2D
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Charcot-Marie-Tooth disease neuronal type 2D
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Charcot-Marie-Tooth neuropathy type 2D
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autosomal dominant Charcot-Marie-Tooth disease type 2D
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Homo sapiens (human)
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DOID:0110163
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Charcot-Marie-Tooth disease axonal type 2F
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Aliases:
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CMT2F
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Charcot-Marie-Tooth neuronal type 2F
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Charcot-Marie-Tooth neuropathy type 2F
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autosomal dominant Charcot-Marie-Tooth disease type 2F
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Homo sapiens (human)
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DOID:0110161
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Charcot-Marie-Tooth disease type 2R
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Aliases:
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CMT2R
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Charcot-Marie-Tooth neuropathy type 2R
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autosomal recessive axonal Charcot-Marie-Tooth disease type 2R
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Homo sapiens (human)
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DOID:0110160
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Charcot-Marie-Tooth disease axonal type 2T
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Aliases:
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AR-CMT2T
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CMT2T
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Charcot-Marie-Tooth neuropathy type 2T
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autosomal recessive axonal Charcot-Marie-Tooth disease type 2T
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Homo sapiens (human)
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DOID:0110159
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Charcot-Marie-Tooth disease type 2B
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Aliases:
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CMT2B
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Charcot-Marie-Tooth neuropathy type 2B
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HMSN IIB
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HMSN2B
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autosomal dominant Charcot-Marie-Tooth disease type 2B
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hereditary motor and sensory nueropathy IIB
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Homo sapiens (human)
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DOID:0110158
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Charcot-Marie-Tooth disease type 2I
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Aliases:
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CMT2I
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Charcot-Marie-Tooth neuropathy type 2I
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Homo sapiens (human)
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DOID:0110157
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Charcot-Marie-Tooth disease type 2J
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Aliases:
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CMT2J
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Charcot-Marie-Tooth disease type 2 with hearing loss and pupillary abnormalities
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Charcot-Marie-Tooth neuropathy type 2J
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Homo sapiens (human)
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DOID:0110156
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Charcot-Marie-Tooth disease type 2B1
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Aliases:
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CMT2B1
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Charcot-Marie-Tooth disease neuronal type 2B1
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Charcot-Marie-Tooth neuropathy type 2B1
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autosomal recessive Charcot-Marie-Tooth disease type 2B1
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autosomal recessive axonal CMT4C1
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autosomal recessive axonal Charcot-Marie-Tooth disease type 2B1
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Homo sapiens (human)
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DOID:0110155
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Charcot-Marie-Tooth disease type 2A2A
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Aliases:
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CMT2A2A
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Charcot-Marie-Tooth neuronal type 2A2
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Charcot-Marie-Tooth neuropathy type 2A2
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HMSN IIA2
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HMSN2A2
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autosomal dominant axonal Charcot-Marie-Tooth disease type 2A2
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hereditary motor and sensory neuropathy IIA2
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Homo sapiens (human)
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DOID:0110154
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Charcot-Marie-Tooth disease type 2A1
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Aliases:
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CMT2A1
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Charcot-Marie-Tooth disease neuronal type 2A1
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Charcot-Marie-Tooth neuropathy type 2A1
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HMSN IIA1
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HMSN2A1
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autosomal dominant Charcot-Marie-Tooth disease axonal type 2A1
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hereditary motor and sensory neuropathy IIA1
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Homo sapiens (human)
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DOID:0110153
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Charcot-Marie-Tooth disease type 1E
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Aliases:
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CMT1E
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Charcot-Marie-Tooth disease and deafness
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Charcot-Marie-Tooth disease demyelinating type 1E
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Charcot-Marie-Tooth disease-deafness
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autosomal dominant Charcot-Marie-Tooth neuropathy and deafness
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Homo sapiens (human)
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DOID:0110152
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Charcot-Marie-Tooth disease type 1B
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Aliases:
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CMT1B
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Charcot-Marie-Tooth disease slow nerve conduction type linked to Duffy
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Charcot-Marie-Tooth neuropathy type 1B
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HMSN IB
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HMSN1B
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autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B
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hereditary motor and sensory neuropathy IB
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peroneal muscular atrophy
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Homo sapiens (human)
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DOID:0110151
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Charcot-Marie-Tooth disease type 1C
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Aliases:
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CMT slow nerve conduction type C
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CMT1C
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Charcot-Marie-Tooth neuropathy type 1C
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HMSN IC
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HMSN1C
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neuropathy hereditary motor and sensory type 1C
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Homo sapiens (human)
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DOID:0110150
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Charcot-Marie-Tooth disease type 1D
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Aliases:
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CMT1D
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Charcot-Marie-Tooth neuropathy type 1D
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HMSN ID
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HMSN1D
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hereditary motor and sensory neuropathy 1D
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Homo sapiens (human)
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DOID:0110149
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Charcot-Marie-Tooth disease type 1F
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Aliases:
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CMT1F
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Charcot-Marie-Tooth neuropathy type 1F
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Homo sapiens (human)
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DOID:0110148
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Charcot-Marie-Tooth disease type 1A
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Aliases:
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CMT1A
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Charcot-Marie-Tooth neuropathy type 1A
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HMSN1A
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autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1A
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hereditary motor and sensory neuropathy 1A
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microduplication 17p12
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Homo sapiens (human)
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