Details of Disease

General Information of Disease (ID: DISNJ929)

Disease Name Myopia 28, autosomal recessive
Synonyms MYP28; myopia 28, autosomal recessive
Disease Hierarchy
DISK5S60: Myopia
DISNJ929: Myopia 28, autosomal recessive
Disease Identifiers
MONDO ID
MONDO_0030697
UMLS CUI
C5676935
OMIM ID
619781
MedGen ID
1806812

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
LOXL3 OTLLY1QI Limited Unknown [1]
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References

1 Exome sequencing identified null mutations in LOXL3 associated with early-onset high myopia. Mol Vis. 2016 Feb 20;22:161-7. eCollection 2016.