DOID:0110190
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Charcot-Marie-Tooth disease type 4B2
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Aliases:
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CMT4B2
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Charcot-Marie-Tooth neuropathy type 4B2
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autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B2
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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:0110207
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Charcot-Marie-Tooth disease X-linked dominant 6
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Aliases:
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CMT6X
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CMTX6
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Charcot-Marie-Tooth neuropathy X-linked dominant 6
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X-linked Charcot-Marie-Tooth disease type 6
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Homo sapiens (human)
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DOID:0110209
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Charcot-Marie-Tooth disease X-linked dominant 1
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Aliases:
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CMT1X
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CMTX1
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Charcot-Marie-Tooth neuropathy X-linked dominant 1
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X-linked Charcot-Marie-Tooth disease type 1
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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: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: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: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: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: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: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: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: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: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: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:0110211
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Charcot-Marie-Tooth disease X-linked recessive 3
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Aliases:
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CMT3X
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CMTX3
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Charcot-Marie-Tooth neuropathy X-linked recessive 3
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X-linked Charcot-Marie-Tooth disease type 3
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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: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: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: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: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: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: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:0110210
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Charcot-Marie-Tooth disease X-linked recessive 5
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Aliases:
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CMT5X
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CMTX5
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Charcot-Marie-Tooth neuropathy X-linked recessive 5
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Rosenberg-Chutorian syndrome
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X-linked Charcot-Marie-Tooth disease type 5
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optic atrophy, polyneuropathy, and deafness
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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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