Search Results

Searched for "Eye Diseases".

1. SOX2 anophthalmia syndrome condition summary
   Related classification: Eye Diseases

   Related genes:

   • SOX2
2. Stickler syndrome condition summary
   Found related term in name or synonym: hereditary arthro-ophthalmopathy

   Related genes:

   • COL11A1
   • COL11A2
   • COL2A1
   • COL9A1
   • COL9A2
3. Lenz microphthalmia syndrome condition summary
   Related classification: Eye Diseases, Hereditary

   Related genes:

   • BCOR
4. Weill-Marchesani syndrome condition summary
   Related classification: Eye Diseases, Hereditary

   Related genes:

   • ADAMTS10
   • FBN1
5. oculofaciocardiodental syndrome condition summary
   Related classification: Eye Diseases, Hereditary

   Related genes:

   • BCOR
6. congenital stromal corneal dystrophy condition summary
   Related classification: Eye Diseases, Hereditary

   Related genes:

   • DCN
7. Norrie disease condition summary
   Related classification: Eye Diseases, Hereditary

   Related genes:

   • NDP
8. lattice corneal dystrophy type I condition summary
   Related classification: Eye Diseases, Hereditary

   Related genes:

   • TGFBI
9. aniridia condition summary
   Related classification: Eye Diseases, Hereditary

   Related genes:

   • PAX6
10. X-linked juvenile retinoschisis condition summary
    Related classification: Eye Diseases

    Related genes:

    • RS1
11. Axenfeld-Rieger syndrome condition summary
    Related classification: Eye Diseases

    Related genes:

    • FOXC1
    • PITX2
12. choroideremia condition summary
    Related classification: Eye Diseases, Hereditary

    Related genes:

    • CHM
13. coloboma condition summary
    Related classification: Eye Diseases
14. gyrate atrophy of the choroid and retina condition summary
    Related classification: Eye Diseases

    Related genes:

    • OAT
15. Horner syndrome condition summary
    Related classification: Eye Diseases
16. Kearns-Sayre syndrome condition summary
    Related classification: Eye Diseases

    Related chromosomes:

    • mitochondrial DNA
17. Leber hereditary optic neuropathy condition summary
    Related classification: Eye Diseases, Hereditary

    Related genes and chromosomes:

    • mitochondrial DNA
    • MT-ND1
    • MT-ND4
    • MT-ND4L
    • MT-ND6
18. microphthalmia with linear skin defects syndrome condition summary
    Related classification: Eye Diseases

    Related genes and chromosomes:

    • X chromosome
    • HCCS
19. microphthalmia condition summary
    Related classification: Eye Diseases
20. ocular albinism condition summary
    Related classification: Eye Diseases, Hereditary

    Related genes:

    • GPR143