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:0050539
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Charcot-Marie-Tooth disease type 2
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Aliases:
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hereditary motor and sensory neuropathy Guadalajara neuronal type
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hereditary motor and sensory neuropathy Okinawa type
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hereditary motor and sensory neuropathy type 2
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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: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: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: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: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: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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DOID:0110203
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Charcot-Marie-Tooth disease recessive intermediate D
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Aliases:
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CMTRID
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RI-CMT type D
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autosomal recessive intermediate Charcot-Marie-Tooth disease type D
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Homo sapiens (human)
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DOID:0110198
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Charcot-Marie-Tooth disease recessive intermediate C
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Aliases:
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CMTRIC
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RI-CMT type C
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RI-CMTC
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autosomal recessive intermediate Charcot-Marie-Tooth disease type C
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Homo sapiens (human)
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DOID:0110204
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Charcot-Marie-Tooth disease recessive intermediate B
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Aliases:
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CMTRIB
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Charcot-Marie-Tooth neuropathy recessive intermediate B
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RI-CMTB
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autosomal recessive intermediate Charcot-Marie-Tooth disease type B
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Homo sapiens (human)
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DOID:0110206
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Charcot-Marie-Tooth disease dominant intermediate F
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Aliases:
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CMTDIF
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autosomal dominant intermediate Charcot-Marie-Tooth disease type F
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Homo sapiens (human)
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DOID:0110205
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Charcot-Marie-Tooth disease dominant intermediate E
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Aliases:
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CMTDIE
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Charcot-Marie-Tooth disease-nephropathy syndrome
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Charcot-Marie-Tooth neuropathy with focal segmental glomerulonephritis
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autosomal dominant intermediate Charcot-Marie-Tooth disease type E
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Homo sapiens (human)
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DOID:0110200
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Charcot-Marie-Tooth disease dominant intermediate D
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Aliases:
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CMTDID
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Charcot-Marie-Tooth neuropathy dominant intermediate D
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DI-CMTD
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autosomal dominant intermediate Charcot-Marie-Tooth disease type D
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Homo sapiens (human)
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DOID:0110199
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Charcot-Marie-Tooth disease dominant intermediate C
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Aliases:
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CMTDIC
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Charcot-Marie-Tooth neuropathy dominant intermediate C
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DI-CMTC
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autosomal dominant intermediate Charcot-Marie-Tooth disease type C
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Homo sapiens (human)
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DOID:0110197
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Charcot-Marie-Tooth disease dominant intermediate B
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Aliases:
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CMTDI1
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CMTDIB
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Charcot-Marie-Tooth neuropathy dominant intermediate B
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DI-CMTB
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Homo sapiens (human)
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DOID:0110202
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Charcot-Marie-Tooth disease dominant intermediate A
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Aliases:
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CMTDIA
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Charcot-Marie-Tooth neuropathy dominant intermediate A
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DI-CMTA
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autosomal dominant intermediate Charcot-Marie-Tooth disease type A
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Homo sapiens (human)
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DOID:0110178
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Charcot-Marie-Tooth disease axonal type 2V
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Aliases:
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CMT2V
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Charcot-Marie-Tooth neuropathy type 2V
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autosomal dominant Charcot-Marie-Tooth disease type 2V
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autosomal dominant axonal Charcot-Marie-Tooth disease type 2V
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Homo sapiens (human)
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DOID:0110173
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Charcot-Marie-Tooth disease axonal type 2U
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Aliases:
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CMT2U
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Charcot-Marie-Tooth neuropathy type 2U
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autosomal dominant Charcot-Marie-Tooth disease type 2U
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autosomal dominant axonal Charcot-Marie-Tooth disease type 2U
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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: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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Homo sapiens (human)
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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:0110175
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Charcot-Marie-Tooth disease axonal type 2O
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Aliases:
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Charcot-Marie-Tooth neuropathy axonal type 2O
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autosomal dominant Charcot-Marie-Tooth disease type 2O
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autosomal dominant axonal Charcot-Marie-Tooth disease type 2O
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Homo sapiens (human)
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DOID:0110177
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Charcot-Marie-Tooth disease axonal type 2N
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Aliases:
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CMT2N
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Charcot-Marie-Tooth neuropathy axonal type 2N
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autosomal dominant Charcot-Marie-Tooth disease type 2N
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autosomal dominant axonal Charcot-Marie-Tooth disease type 2N
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Homo sapiens (human)
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DOID:0110174
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Charcot-Marie-Tooth disease axonal type 2L
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Aliases:
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CMT2L
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Charcot-Marie-Tooth neuropathy axonal type 2L
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autosomal dominant Charcot-Marie-Tooth disease type 2L
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autosomal dominant axonal Charcot-Marie-Tooth disease type 2L
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Homo sapiens (human)
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