Charcot-Marie-Tooth disease axonal type 2Z
- Synonyms
- CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2Z; CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2Z
- Modes of inheritance
- Autosomal dominant inheritance (Orphanet)
Summary
Available tests
Check Related conditions for additional relevant tests.
Clinical tests (11 available)
Genes See tests for all associated and related genes
Also known as: CMT2Z, DIGFAN, ZCW3, ZCWCC1, MORC2
Summary: MORC family CW-type zinc finger 2
Clinical features
Help- Abnormality of limbs
- Absent Achilles reflex
Absent Achilles reflex
- MedGen UID: 108240
- Concept ID: C0558845
- Finding: Finding
Abnormality of limbs
- Foot dorsiflexor weakness
Foot dorsiflexor weakness
- MedGen UID: 356163
- Concept ID: C1866141
- Finding: Finding
Abnormality of limbs
- Pes cavus
Pes cavus
- MedGen UID: 675590
- Concept ID: C0728829
- Finding: Congenital Abnormality
Abnormality of limbs
- Pes planus
Pes planus
- MedGen UID: 42034
- Concept ID: C0016202
- Finding: Anatomical Abnormality
Abnormality of limbs
- Split hand
Split hand
- MedGen UID: 397570
- Concept ID: C2699510
- Finding: Congenital Abnormality
Abnormality of limbs
- Wrist drop
Wrist drop
- MedGen UID: 533950
- Concept ID: C0231666
- Finding: Finding
Abnormality of limbs
- Absent Achilles reflex
- Abnormality of the musculoskeletal system
- Distal amyotrophy
Distal amyotrophy
- MedGen UID: 338530
- Concept ID: C1848736
- Finding: Disease or Syndrome
Abnormality of the musculoskeletal system
- Distal muscle weakness
Distal muscle weakness
- MedGen UID: 140883
- Concept ID: C0427065
- Finding: Finding
Abnormality of the musculoskeletal system
- Hypertonia
Hypertonia
- MedGen UID: 10132
- Concept ID: C0026826
- Finding: Finding
Abnormality of the musculoskeletal system
- Hypotonia
Hypotonia
- MedGen UID: 10133
- Concept ID: C0026827
- Finding: Finding
Abnormality of the musculoskeletal system
- Intrinsic hand muscle atrophy
Intrinsic hand muscle atrophy
- MedGen UID: 351202
- Concept ID: C1864716
- Finding: Finding
Abnormality of the musculoskeletal system
- Muscle spasm
Muscle spasm
- MedGen UID: 52431
- Concept ID: C0037763
- Finding: Sign or Symptom
Abnormality of the musculoskeletal system
- Proximal muscle weakness
Proximal muscle weakness
- MedGen UID: 113169
- Concept ID: C0221629
- Finding: Finding
Abnormality of the musculoskeletal system
- Scoliosis
Scoliosis
- MedGen UID: 11348
- Concept ID: C0036439
- Finding: Disease or Syndrome
Abnormality of the musculoskeletal system
- Distal amyotrophy
- Abnormality of the nervous system
- Abnormal pyramidal sign
Abnormal pyramidal sign
- MedGen UID: 68582
- Concept ID: C0234132
- Finding: Sign or Symptom
Abnormality of the nervous system
- Abnormally high-pitched voice
Abnormally high-pitched voice
- MedGen UID: 66836
- Concept ID: C0241703
- Finding: Finding
Abnormality of the nervous system
- Areflexia
Areflexia
- MedGen UID: 115943
- Concept ID: C0234146
- Finding: Finding
Abnormality of the nervous system
- Babinski sign
Babinski sign
- MedGen UID: 19708
- Concept ID: C0034935
- Finding: Finding
Abnormality of the nervous system
- Cerebellar ataxia
Cerebellar ataxia
- MedGen UID: 849
- Concept ID: C0007758
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Clumsiness
Clumsiness
- MedGen UID: 66690
- Concept ID: C0233844
- Finding: Sign or Symptom
Abnormality of the nervous system
- Decreased amplitude of sensory action potentials
Decreased amplitude of sensory action potentials
- MedGen UID: 870496
- Concept ID: C4024943
- Finding: Finding
Abnormality of the nervous system
- Decreased motor nerve conduction velocity
Decreased motor nerve conduction velocity
- MedGen UID: 388130
- Concept ID: C1858729
- Finding: Finding
Abnormality of the nervous system
- Distal sensory impairment
Distal sensory impairment
- MedGen UID: 335722
- Concept ID: C1847584
- Finding: Finding
Abnormality of the nervous system
- Fasciculations
Fasciculations
- MedGen UID: 5124
- Concept ID: C0015644
- Finding: Sign or Symptom
Abnormality of the nervous system
- Gait ataxia
Gait ataxia
- MedGen UID: 155642
- Concept ID: C0751837
- Finding: Sign or Symptom
Abnormality of the nervous system
- Gait disturbance
Gait disturbance
- MedGen UID: 107895
- Concept ID: C0575081
- Finding: Finding
Abnormality of the nervous system
- Global developmental delay
Global developmental delay
- MedGen UID: 107838
- Concept ID: C0557874
- Finding: Finding
Abnormality of the nervous system
- Hyporeflexia
Hyporeflexia
- MedGen UID: 195967
- Concept ID: C0700078
- Finding: Finding
Abnormality of the nervous system
- Impaired distal proprioception
Impaired distal proprioception
- MedGen UID: 867227
- Concept ID: C4021585
- Finding: Finding
Abnormality of the nervous system
- Impaired distal tactile sensation
Impaired distal tactile sensation
- MedGen UID: 867225
- Concept ID: C4021583
- Finding: Finding
Abnormality of the nervous system
- Impaired distal vibration sensation
Impaired distal vibration sensation
- MedGen UID: 381262
- Concept ID: C1853767
- Finding: Finding
Abnormality of the nervous system
- Incoordination
Incoordination
- MedGen UID: 141714
- Concept ID: C0520966
- Finding: Finding
Abnormality of the nervous system
- Motor delay
Motor delay
- MedGen UID: 381392
- Concept ID: C1854301
- Finding: Finding
Abnormality of the nervous system
- Myokymia
Myokymia
- MedGen UID: 146882
- Concept ID: C0684219
- Finding: Sign or Symptom
Abnormality of the nervous system
- Abnormal pyramidal sign
- Constitutional symptom
- Urinary incontinence
Urinary incontinence
- MedGen UID: 22579
- Concept ID: C0042024
- Finding: Finding
Constitutional symptom
- Urinary incontinence
- Ear malformation
- Hearing impairment
Hearing impairment
- MedGen UID: 235586
- Concept ID: C1384666
- Finding: Disease or Syndrome
Ear malformation
- Hearing impairment
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