occult macular dystrophy Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A macular degeneration that is characterized by a central cone dysfunction leading to a loss of vision with a normal fundus and normal fluorescein angiography findings. (Human Disease Ontology, DOID_0050578)
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Genes

7 genes co-occuring with the disease occult macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
RP1L1 retinitis pigmentosa 1-like 1 3.24793
OMD osteomodulin 1.53128
PCM1 pericentriolar material 1 1.41314
MSRA methionine sulfoxide reductase A 1.23429
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4 1.14433
RING1 ring finger protein 1 1.10594
GATA4 GATA binding protein 4 0.739488