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Results: 1 to 20 of 28

1.

Ataxic gait

Impairment of the ability to coordinate the movements required for normal ambulation (WALKING) which may result from impairments of motor function or sensory feedback. This condition may be associated with BRAIN DISEASES (including CEREBELLAR DISEASES and BASAL GANGLIA DISEASES); SPINAL CORD DISEASES; or PERIPHERAL NERVOUS SYSTEM DISEASES. [from MeSH]

MedGen UID:
155642
Concept ID:
C0751837
Sign or Symptom
2.

Tremor, Semirhythmic

MedGen UID:
155884
Concept ID:
C0751565
Finding
3.

Tremor, Limb

MedGen UID:
115980
Concept ID:
C0235081
Sign or Symptom
4.

Tremor, Neonatal

MedGen UID:
68626
Concept ID:
C0235843
Sign or Symptom
5.

Tremor, Perioral

MedGen UID:
66717
Concept ID:
C0235078
Sign or Symptom
6.

Nerve Tremors

MedGen UID:
65898
Concept ID:
C0235083
Sign or Symptom
7.

Tremor, Muscle

MedGen UID:
65897
Concept ID:
C0235082
Sign or Symptom
8.

Gait ataxia

A type of `ataxia` (HP:0001251) characterized by the impairment of the ability to coordinate the movements required for normal walking. [from HPO]

MedGen UID:
505076
Concept ID:
CN001868
Finding
9.

Gait ataxia

MedGen UID:
472347
Concept ID:
CN130269
Disease or Syndrome
10.

Fragile X-associated tremor/ataxia syndrome

MedGen UID:
756479
Concept ID:
C3164069
Disease or Syndrome
11.

Intention tremor

An oscillatory cerebellar ataxia that tends to be absent when the limbs are inactive and during the first part of voluntary movement but worsening as the movement continues and greater precision is required (e.g., in touching a target such as the patient's nose or a physician's finger). [from HPO]

MedGen UID:
505089
Concept ID:
CN001882
Finding
12.

Fragile X tremor/ataxia syndrome

FMR1-related disorders include fragile X syndrome, fragile X-associated tremor/ataxia syndrome (FXTAS), and FMR1-related primary ovarian insufficiency (POI). Fragile X syndrome occurs in individuals with an FMR1 full mutation or other loss-of-function mutation and is nearly always characterized by moderate intellectual disability in affected males and mild intellectual disability in affected females. Because FMR1 mutations are complex alterations involving non-classic gene-disrupting alterations (trinucleotide repeat expansion) and abnormal gene methylation, affected individuals occasionally have an atypical presentation with an IQ above 70, the traditional demarcation denoting intellectual disability (previously referred to as mental retardation). Males with an FMR1 full mutation accompanied by aberrant methylation may have a characteristic appearance (large head, long face, prominent forehead and chin, protruding ears), connective tissue findings (joint laxity), and large testes after puberty. Behavioral abnormalities, sometimes including autism spectrum disorder, are common. FXTAS occurs in males (and some females) who have an FMR1 premutation and is characterized by late-onset, progressive cerebellar ataxia and intention tremor. FMR1-related POI (age at cessation of menses <40 years) occurs in approximately 20% of females who have an FMR1 premutation. [from GeneReviews]

MedGen UID:
333403
Concept ID:
C1839780
Disease or Syndrome
13.

Intention tremor

MedGen UID:
65875
Concept ID:
C0234376
Sign or Symptom
14.

Pineal gland disorder

MedGen UID:
676114
Concept ID:
C0729870
Disease or Syndrome
15.

Disorder of epididymis

MedGen UID:
675113
Concept ID:
C0700113
Disease or Syndrome
16.

Congenital anomaly of epididymis

MedGen UID:
672782
Concept ID:
C0685857
Congenital Abnormality
17.

Finding of thyroid gland

MedGen UID:
662148
Concept ID:
C0578743
Finding
18.

Mitral valve finding

MedGen UID:
661277
Concept ID:
C0577791
Finding
19.

Heart valve finding

MedGen UID:
661274
Concept ID:
C0577788
Finding
20.

Somatic syndrome present

MedGen UID:
631664
Concept ID:
C0459437
Finding

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