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12 Result(s)

ORPHA:401964   (Disorder)   Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons

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Synonym(s) : HMSN2 with giant axons

ORPHA:476109   (Group of disorders)   Axonal hereditary motor and sensory neuropathy

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Synonym(s) : Axonal HMSN

ORPHA:99950   (Disorder)   Charcot-Marie-Tooth disease type 4D

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Synonym(s) : HMSN, Lom type

ORPHA:99953   (Disorder)   Charcot-Marie-Tooth disease type 4G

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Synonym(s) : HMSNR

ORPHA:166   (Group of disorders)   Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy

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Synonym(s) : CMT/HMSN

ORPHA:64748   (Disorder)   Dejerine-Sottas syndrome

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Synonym(s) : HMSN III

ORPHA:476116   (Group of disorders)   Demyelinating hereditary motor and sensory neuropathy

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Synonym(s) : Demyelinating HMSN

ORPHA:64751   (Disorder)   Hereditary motor and sensory neuropathy type 5

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Synonym(s) : HMSN V

ORPHA:90120   (Disorder)   Hereditary motor and sensory neuropathy type 6

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Synonym(s) : HMSN VI

ORPHA:90119   (Disorder)   Hereditary motor and sensory neuropathy with acrodystrophy

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Synonym(s) : HMSN with acrodystrophy

ORPHA:90117   (Disorder)   Hereditary motor and sensory neuropathy, Okinawa type

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Synonym(s) : HMSNP

ORPHA:773   (Disorder)   Refsum disease

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Synonym(s) : HMSN IV