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: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: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:0110187
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Charcot-Marie-Tooth disease type 4K
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Aliases:
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CMT4K
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SURF1-related CMT4
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SURF1-related Charcot-Marie-Tooth disease type 4
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SURF1-related severe demyelinating Charcot-Marie-Tooth disease
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autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4K
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autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy type 4K
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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: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: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: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: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: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: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:0110165
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Charcot-Marie-Tooth disease type 2E
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Aliases:
-
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: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: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:0110204
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Charcot-Marie-Tooth disease recessive intermediate B
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Aliases:
-
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: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: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: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:0110190
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Charcot-Marie-Tooth disease type 4B2
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Aliases:
-
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: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:5418
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|
|
|
Homo sapiens (human)
|
|
DOID:11328
|
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schizophreniform disorder
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|
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Homo sapiens (human)
|
|
DOID:2491
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sensory peripheral neuropathy
-
Aliases:
-
peripheral Sensory Neuropathy
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sensory neuropathy
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|
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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
-
hereditary motor and sensory neuropathy type 2
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Homo sapiens (human)
|
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