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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DOID:2477
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motor peripheral neuropathy
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Aliases:
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HSMN
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HSMN - Hereditary sensory and motor neuropathy
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Hereditary motor and sensory neuropathy
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Peripheral Motor Neuropathy
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neuropathic muscular atrophy
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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:0110186
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Charcot-Marie-Tooth disease type 4D
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Aliases:
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CMT4D
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Charcot-Marie-Tooth neuropathy type 4D
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HMSN Lom type
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HMSN-Lom
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HMSN4D
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HMSNL
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autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4D
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hereditary motor and sensory neuropathy LOM type
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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: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: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:0110208
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Charcot-Marie-Tooth disease X-linked recessive 2
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Aliases:
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CMTX2
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Charcot-Marie-Tooth neuropathy X-linked recessive 2
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X-linked Charcot-Marie-Tooth disease type 2
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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: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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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: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: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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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: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: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:0110182
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Charcot-Marie-Tooth disease axonal type 2C
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Aliases:
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CMT2C
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Charcot-Marie-Tooth neuropathy type 2C
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HMSN2C
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autosomal cominant axonal Charcot-Marie-Tooth disease type 2C
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autosomal dominant Charcot-Marie-Tooth disease type 2C
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hereditary motor and sensory neuropathy type IIc
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Homo sapiens (human)
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