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Items: 6

1.

Intermediate uveitis

Inflammation of the pars plana, ciliary body, and adjacent structures. [from MeSH]

MedGen UID:
22596
Concept ID:
C0042166
Disease or Syndrome
2.

Pars planitis

An inflammatory disorder of the cilliary body in the uvea that affects healthy, younger individuals who are often asymptomatic. It has a long clinical course with relapses and remissions. Symptoms include mildly decreased vision and floaters. It may be associated with autoimmune disorders. [from NCI]

MedGen UID:
14623
Concept ID:
C0030593
Disease or Syndrome
3.

Lens subluxation

A partial dislocation of the lens of the eye. [from NCI]

MedGen UID:
9718
Concept ID:
C0023316
Disease or Syndrome
4.

Hypermature cataract

MedGen UID:
508950
Concept ID:
C0152258
Disease or Syndrome
5.

Zonular dehiscence

Rupture of the fibrous strands connecting the ciliary body and the crystalline lens of the eye. [from NCI]

MedGen UID:
226971
Concept ID:
C1299683
Finding
6.

Cataract, zonular

Congenital cataracts cause 10 to 30% of all blindness in children, with one-third of cases estimated to have a genetic cause (summary by Bu et al., 2002). Mutations in the HSF4 gene have been found to cause multiple types of cataract, which have been described as infantile, lamellar, zonular, nuclear, anterior polar, stellate, and Marner-type. The preferred title for this entry was formerly 'Lamellar Cataract,' with 'Cataract, Marner Type; CAM; CTM' an included title. [from GTR]

MedGen UID:
78608
Concept ID:
C0266537
Congenital Abnormality; Finding
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