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Items: 1 to 20 of 27

1.

Seizure

MedGen UID:
506957
Concept ID:
CN178372
Disease or Syndrome
2.

Diamond-Blackfan anemia

Diamond-Blackfan anemia (DBA) in its classic form is characterized by a profound normochromic and usually macrocytic anemia with normal leukocytes and platelets, congenital malformations in up to 50% of affected individuals, and growth retardation in 30% of affected individuals. The hematologic complications occur in 90% of affected individuals during the first year of life. The phenotypic spectrum ranges from a mild form (e.g., mild anemia, no anemia with only subtle erythroid abnormalities, physical malformations without anemia) to a severe form of fetal anemia resulting in nonimmune hydrops fetalis. DBA is associated with an increased risk for acute myelogenous leukemia (AML), myelodysplastic syndrome (MDS), and solid tumors including osteogenic sarcoma. [from GTR]

MedGen UID:
266045
Concept ID:
C1260899
Disease or Syndrome
3.

Seizures

Clinical or subclinical disturbances of cortical function due to a sudden, abnormal, excessive, and disorganized discharge of brain cells. Clinical manifestations include abnormal motor, sensory and psychic phenomena. Recurrent seizures are usually referred to as EPILEPSY or "seizure disorder." [from MeSH]

MedGen UID:
20693
Concept ID:
C0036572
Sign or Symptom
4.

Convulsion

MedGen UID:
885903
Concept ID:
C4048158
Sign or Symptom
5.

Channelopathies

A variety of neuromuscular conditions resulting from MUTATIONS in ION CHANNELS manifesting as episodes of EPILEPSY; HEADACHE DISORDERS; and DYSKINESIAS. [from MeSH]

MedGen UID:
328427
Concept ID:
C1720983
Disease or Syndrome
6.

Disease Attributes

Clinical characteristics of disease or illness. [from MeSH]

MedGen UID:
199876
Concept ID:
C0752357
Disease or Syndrome
7.

Focal seizures

A transitory alteration in movement, sensation or autonomic nerve function due to abnormal electric activity in a localized area of the cerebral cortex, usually without change in awareness or alertness. Symptoms vary with different lesion locations and may include but not limited to the motor (e.g. rhythmic muscle contractions in one area of the body), somatosensory and sensory alterations manifested by abnormal numbness, paresthesias or other hallucinations, including several types of aura; autonomic and psychic symptoms, e.g. with changes in speech, thought, personality, mood, sensation of deja vu or hallucinations. [from NCI]

MedGen UID:
199670
Concept ID:
C0751495
Disease or Syndrome
8.

Seizures, Sensory

MedGen UID:
155571
Concept ID:
C0751496
Sign or Symptom
9.

Convulsion, Non-Epileptic

MedGen UID:
148227
Concept ID:
C0751056
Sign or Symptom
10.

Generalized tonic-clonic seizures

A generalized tonic-clinic seizure, characterized by loss of consciousness. This type of seizure may be preceded by an aura and is frequently followed by a period of confusion and lethargy (post-ictal state). [from NCI]

MedGen UID:
141670
Concept ID:
C0494475
Disease or Syndrome; Finding
11.

Olfactory seizure

MedGen UID:
140831
Concept ID:
C0422853
Disease or Syndrome
12.

Somatosensory seizure

MedGen UID:
140830
Concept ID:
C0422850
Pathologic Function
13.

Genetic predisposition

A latent susceptibility to disease at the genetic level, which may be activated under certain conditions. [from MeSH]

MedGen UID:
137259
Concept ID:
C0314657
Organism Attribute
14.

Generalized seizures

Seizures of with initial involvement of both cerebral hemispheres. [from HPO]

MedGen UID:
115963
Concept ID:
C0234533
Disease or Syndrome
15.

Epileptic vertigo

MedGen UID:
98062
Concept ID:
C0422855
Disease or Syndrome
16.

Gustatory Seizures

MedGen UID:
98061
Concept ID:
C0422854
Sign or Symptom
17.

Auditory seizure

MedGen UID:
98060
Concept ID:
C0422852
Pathologic Function
18.

Mutagenesis

Process of generating a genetic MUTATION. It may occur spontaneously or be induced by MUTAGENS. [from MeSH]

MedGen UID:
86969
Concept ID:
C0079866
Molecular Function
19.

Tonic seizure

Prolonged contraction of the muscles, as the result of an epileptic discharge. [from NCI]

MedGen UID:
82855
Concept ID:
C0270844
Sign or Symptom
20.

Visual epilepsy

MedGen UID:
75723
Concept ID:
C0270824
Disease or Syndrome
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