blindness

Summary
Synonym
  • vision impairment
  • vision loss
  • visual impairment
Definition
An eye disease characterized by a lack or loss of vision.
Super Class
eye disease
Disease Ontology
DOID:1432
Mondo Disease Ontology
UMLS
MGI genotype (from TogoID)
Related Genes
Displaying all 7 entries
Gene ID Gene Symbol Description Source
361 AQP4 aquaporin 4
6154 RPL26 ribosomal protein L26
8992 ATP6V0E1 ATPase H+ transporting V0 subunit e1
10908 PNPLA6 patatin like phospholipase domain containing 6
51168 MYO15A myosin XVA
57709 SLC7A14 solute carrier family 7 member 14
375775 PNPLA7 patatin like phospholipase domain containing 7
Displaying all 5 entries
Gene ID Gene Symbol Description Source
11829 Aqp4 aquaporin 4
11974 Atp6v0e ATPase, H+ transporting, lysosomal V0 subunit E
19941 Rpl26 ribosomal protein L26
50767 Pnpla6 patatin-like phospholipase domain containing 6
241919 Slc7a14 solute carrier family 7 (cationic amino acid transporter, y+ system), member 14
Displaying 1 entry
Gene ID Gene Symbol Description Source
25293 Aqp4 aquaporin 4
Displaying all 4 entries
Gene ID Gene Symbol Description Source
850665 MMP1 S-methylmethionine permease MMP1
854530 PUT4 proline permease PUT4
854943 NTE1 lysophospholipase
855854 SAM3 bifunctional polyamine/amino acid permease SAM3

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024