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Leber congenital amaurosis 14 | RareConnect | RareConnect.io

/Leber congenital amaurosis

/Leber congenital amaurosis 14

Leber congenital amaurosis 14

Rare Disease

MONDO:0013231

Also Known As

LCA14LRAT Leber congenital amaurosisLeber congenital amaurosis 14Leber congenital amaurosis caused by mutation in LRATLeber congenital amaurosis type 14retinal dystrophy, early-onset severeretinal dystrophy, early-onset Severe, LRAT-relatedretinitis pigmentosa, juvenileretinitis pigmentosa, juvenile, LRAT-related

Definition

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the LRAT gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:613341 ↗

GARD

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