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Items: 13

1.

Encephalopathy, mitochondrial

A type of ataxia characterized by the impairment of the ability to smoothly perform the elements of a voluntary movement in the appropriate order and speed. With dyssynergia, a voluntary movement appears broken down into its component parts. [from GeneReviews]

MedGen UID:
342221
Concept ID:
C1852373
Disease or Syndrome
2.

Ataxia

A type of ataxia characterized by the impairment of the ability to smoothly perform the elements of a voluntary movement in the appropriate order and speed. With dyssynergia, a voluntary movement appears broken down into its component parts. [from GeneReviews]

MedGen UID:
13945
Concept ID:
C0004134
Sign or Symptom
3.

Abnormality of mitochondrial metabolism

A type of ataxia characterized by the impairment of the ability to smoothly perform the elements of a voluntary movement in the appropriate order and speed. With dyssynergia, a voluntary movement appears broken down into its component parts. [from GeneReviews]

MedGen UID:
867369
Concept ID:
C4021734
Finding
4.

Ataxia

A type of ataxia characterized by the impairment of the ability to smoothly perform the elements of a voluntary movement in the appropriate order and speed. With dyssynergia, a voluntary movement appears broken down into its component parts. [from GeneReviews]

MedGen UID:
504767
Concept ID:
CN001146
Finding
5.

Abnormality of mitochondrial metabolism

A type of ataxia characterized by the impairment of the ability to smoothly perform the elements of a voluntary movement in the appropriate order and speed. With dyssynergia, a voluntary movement appears broken down into its component parts. [from GeneReviews]

MedGen UID:
446482
Concept ID:
CN002968
Finding
6.

Friedreich ataxia 1

A type of ataxia characterized by the impairment of the ability to smoothly perform the elements of a voluntary movement in the appropriate order and speed. With dyssynergia, a voluntary movement appears broken down into its component parts. [from GeneReviews]

MedGen UID:
383962
Concept ID:
C1856689
Disease or Syndrome
7.

Friedreich ataxia

A type of ataxia characterized by the impairment of the ability to smoothly perform the elements of a voluntary movement in the appropriate order and speed. With dyssynergia, a voluntary movement appears broken down into its component parts. [from GeneReviews]

MedGen UID:
5276
Concept ID:
C0016719
Disease or Syndrome
8.

Mitochondrial diseases

A type of ataxia characterized by the impairment of the ability to smoothly perform the elements of a voluntary movement in the appropriate order and speed. With dyssynergia, a voluntary movement appears broken down into its component parts. [from GeneReviews]

MedGen UID:
155901
Concept ID:
C0751651
Disease or Syndrome
9.

Neurodegenerative disease

A type of ataxia characterized by the impairment of the ability to smoothly perform the elements of a voluntary movement in the appropriate order and speed. With dyssynergia, a voluntary movement appears broken down into its component parts. [from GeneReviews]

MedGen UID:
101195
Concept ID:
C0524851
Disease or Syndrome
10.

Metabolic disease

A type of ataxia characterized by the impairment of the ability to smoothly perform the elements of a voluntary movement in the appropriate order and speed. With dyssynergia, a voluntary movement appears broken down into its component parts. [from GeneReviews]

MedGen UID:
44376
Concept ID:
C0025517
Disease or Syndrome
11.

Myelopathy

A type of ataxia characterized by the impairment of the ability to smoothly perform the elements of a voluntary movement in the appropriate order and speed. With dyssynergia, a voluntary movement appears broken down into its component parts. [from GeneReviews]

MedGen UID:
11550
Concept ID:
C0037928
Disease or Syndrome
12.

Disorder of the central nervous system

A type of ataxia characterized by the impairment of the ability to smoothly perform the elements of a voluntary movement in the appropriate order and speed. With dyssynergia, a voluntary movement appears broken down into its component parts. [from GeneReviews]

MedGen UID:
3306
Concept ID:
C0007682
Disease or Syndrome
13.

Hereditary ataxia

A type of ataxia characterized by the impairment of the ability to smoothly perform the elements of a voluntary movement in the appropriate order and speed. With dyssynergia, a voluntary movement appears broken down into its component parts. [from GeneReviews]

MedGen UID:
2478
Concept ID:
C0004138
Disease or Syndrome
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