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Items: 8

1.

Cervical rib

A supernumerary rib developing from an abnormal enlargement of the costal element of the C7 vertebra. This anomaly is found in 1-2% of the population and can put pressure on adjacent structures causing CERVICAL RIB SYNDROME; THORACIC OUTLET SYNDROME; or other conditions. [from MeSH]

MedGen UID:
102359
Concept ID:
C0158779
Congenital Abnormality
2.

Stroke

A group of pathological conditions characterized by sudden, non-convulsive loss of neurological function due to BRAIN ISCHEMIA or INTRACRANIAL HEMORRHAGES. Stroke is classified by the type of tissue NECROSIS, such as the anatomic location, vasculature involved, etiology, age of the affected individual, and hemorrhagic vs. non-hemorrhagic nature. (From Adams et al., Principles of Neurology, 6th ed, pp777-810) [from MeSH]

MedGen UID:
52522
Concept ID:
C0038454
Disease or Syndrome
3.

Episodic

Applied to a sign, symptom, or other manifestation that occurs at least twice and potentially multiple times but separated by an interval in whichthe sign, symptom, or manifestation is not present. [from HPO]

MedGen UID:
910017
Concept ID:
CN240220
Organism Attribute
4.

Stroke

MedGen UID:
340407
Concept ID:
C1849743
5.

Very rare

MedGen UID:
344528
Concept ID:
C1855575
Finding
6.

Subclavian steal syndrome

A clinically significant reduction in blood supply to the BRAIN STEM and CEREBELLUM (i.e., VERTEBROBASILAR INSUFFICIENCY) resulting from reversal of blood flow through the VERTEBRAL ARTERY from occlusion or stenosis of the proximal subclavian or brachiocephalic artery. Common symptoms include VERTIGO; SYNCOPE; and INTERMITTENT CLAUDICATION of the involved upper extremity. Subclavian steal may also occur in asymptomatic individuals. (From J Cardiovasc Surg 1994;35(1):11-4; Acta Neurol Scand 1994;90(3):174-8) [from MeSH]

MedGen UID:
20983
Concept ID:
C0038531
Disease or Syndrome
7.

Arterial thoracic outlet syndrome due to cervical rib

Thoracic outlet syndrome, either nerve or vessel compression, due to a cervical rib [from SNOMEDCT_US]

MedGen UID:
3337
Concept ID:
C0007856
Disease or Syndrome
8.

Left hemiparesis

MedGen UID:
630100
Concept ID:
C0457436
Finding
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