Additional Disease Briefs

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Rare Disease Database Reports Additional Rare Disease Briefs
Charcot-Marie-Tooth disease type 4C

Also known as: CMT 4C, CMT4C, Charcot Marie Tooth disease type 4C, Charcot-Marie-Tooth disease type 4 caused by mutation in SH3TC2, Charcot-Marie-Tooth disease type 4C, Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4C, Charcot-Marie-Tooth disease, type 4C, Charcot-Marie-Tooth neuropathy type 4C, Charcot-Marie-Tooth neuropathy, type 4C, SH3TC2 Charcot-Marie-Tooth disease type 4, autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4C

Charcot-Marie-Tooth disease type 4D

Also known as: CMT4D, Charcot-Marie-Tooth disease type 4 caused by mutation in NDRG1, Charcot-Marie-Tooth disease type 4D, Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4D, Charcot-Marie-Tooth disease, type 4D, Charcot-Marie-Tooth neuropathy type 4D, Charcot-Marie-Tooth neuropathy, type 4D, HMSN Lom type, HMSN, Lom type, HMSN-Lom, HMSN4D, HMSNL, NDRG1 Charcot-Marie-Tooth disease type 4, NMSL, autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4D, hereditary motor ABD sensory neuropathy Lom type, hereditary motor and sensory neuropathy, Lom type, neuropathy, hereditary motor and sensory, Lom type

Charcot-Marie-Tooth disease type 4F

Also known as: CMT4F, Charcot-Marie-Tooth disease type 4 caused by mutation in PRX, Charcot-Marie-Tooth disease type 4 caused by mutation in Prx, Charcot-Marie-Tooth disease, demyelinating, type 4F, Charcot-Marie-Tooth disease, type 4F, PRX Charcot-Marie-Tooth disease type 4, Prx Charcot-Marie-Tooth disease type 4

Charcot-Marie-Tooth disease type 4G

Also known as: CMT4G, Charcot-Marie-Tooth disease type 4 caused by mutation in HK1, Charcot-Marie-Tooth disease, autosomal recessive, type 4G, Charcot-Marie-Tooth disease, type 4G, Charcot-Marie-Tooth neuropathy type 4G, Charcot-Marie-Tooth neuropathy, type 4G, HK1 Charcot-Marie-Tooth disease type 4, HMSNR, autosomal recessive Charcot-Marie-Tooth disease type 4G, hereditary motor and sensory neuropathy Russe type, hereditary motor and sensory neuropathy, Russe type, neuropathy, hereditary motor and sensory, Russe type

Charcot-Marie-Tooth disease type 4H

Also known as: CMT4H, Charcot-Marie-Tooth disease type 4 caused by mutation in FGD4, Charcot-Marie-Tooth disease type 4H, Charcot-Marie-Tooth disease, autosomal recessive, type 4H, Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4H, Charcot-Marie-Tooth disease, type 4H, Charcot-Marie-Tooth neuropathy type 4H, Charcot-Marie-Tooth neuropathy, type 4H, FGD4 Charcot-Marie-Tooth disease type 4, autosomal recessive Charcot-Marie-Tooth disease type 4H, autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4H

Charcot-Marie-Tooth disease type 4J

Also known as: CMT4J, Charcot-Marie-Tooth disease type 4 caused by mutation in FIG4, Charcot-Marie-Tooth disease, autosomal recessive, type 4J, Charcot-Marie-Tooth disease, type 4J, FIG4 Charcot-Marie-Tooth disease type 4, autosomal recessive Charcot-Marie-Tooth disease type 4J

Charcot-Marie-Tooth disease type 4K

Also known as: CMT4K, Charcot-Marie-Tooth disease type 4 caused by mutation in SURF1, Charcot-Marie-Tooth disease type 4K, Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4K, Charcot-Marie-Tooth disease, type 4K, Charcot-Marie-Tooth disease, type 4k, Charcot-Marie-Tooth neuropathy, demyelinating, autosomal recessive, type 4K, SURF1 Charcot-Marie-Tooth disease type 4, SURF1-related CMT4, SURF1-related Charcot-Marie-Tooth disease type 4, SURF1-related severe demyelinating Charcot-Marie-Tooth disease, autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4K, autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy type 4K

Charcot-Marie-Tooth disease type 5

Also known as: CMT with pyramidal features, Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant, Charcot-Marie-Tooth disease-pyramidal features syndrome, Charcot-Marie-Tooth neuropathy with pyramidal features, autosomal dominant, HMSN 5, HMSN5, hereditary motor and sensory neuropathy 5, hereditary motor and sensory neuropathy V, hereditary motor and sensory neuropathy type 5, hereditary motor and sensory neuropathy with pyramidal features, peroneal muscular atrophy with pyramidal features, autosomal dominant

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