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: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: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:0110185
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Charcot-Marie-Tooth disease type 4A
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Aliases:
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CMT4A
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Charcot-Marie-Tooth neuropathy type 4A
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autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4A
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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: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: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: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: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: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: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: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:0110196
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Charcot-Marie-Tooth disease type 4G
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Aliases:
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CMT4G
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Charcot-Marie-Tooth neuropathy type 4G
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HMSNR
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autosomal recessive Charcot-Marie-Tooth disease type 4G
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hereditary motor and sensory neuropathy Russe type
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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:0110212
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Charcot-Marie-Tooth disease X-linked recessive 4
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Aliases:
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CMT4X
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CMTX4
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Charcot-Marie-Tooth disease with deafness and mental retardation
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Cowchock syndrome
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NADMR
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NAMSD
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X-linked Charcot-Marie-Tooth disease type 4
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axonal motor sensory neuropathy with deafness and mental retardation
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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:0110183
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Charcot-Marie-Tooth disease type 4C
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Aliases:
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CMT4C
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Charcot-Marie-Tooth neuropathy type 4C
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autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4C
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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: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:0110184
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Charcot-Marie-Tooth disease type 4J
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Aliases:
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CMT4J
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autosomal recessive Charcot-Marie-Tooth disease type 4J
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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:0110194
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Charcot-Marie-Tooth disease type 4B3
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Aliases:
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Homo sapiens (human)
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DOID:0110195
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Charcot-Marie-Tooth disease type 4E
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Aliases:
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CMT4E
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Charcot-Marie-Tooth neuropathy type 4E
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Neuropathy, congenital hypomyelinating, 1
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autosomal recessive congenital hypomyelinating or amyelinating neuropathy
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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:0110192
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Charcot-Marie-Tooth disease type 4H
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Aliases:
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CMT4H
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Charcot-Marie-Tooth neuropathy type 4H
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autosomal recessive Charcot-Marie-Tooth disease type 4H
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autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4H
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Homo sapiens (human)
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