Details of Disease

General Information of Disease (ID: DISHHVZB)

Disease Name Cataract 19 multiple types
Synonyms cataract 19; cataract 19, multiple types; cataract type 19; LIM2 early-onset non-syndromic cataract; early-onset non-syndromic cataract caused by mutation in LIM2; CTRCT19
Definition Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the LIM2 gene.
Disease Hierarchy
DIS4VPS0: Early-onset non-syndromic cataract
DISHHVZB: Cataract 19 multiple types
Disease Identifiers
MONDO ID
MONDO_0014111
UMLS CUI
C3809004
OMIM ID
615277
MedGen ID
815334

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
LIM2 OTK7R6HC Definitive Autosomal recessive [1]
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References

1 A missense mutation in LIM2 causes autosomal recessive congenital cataract. Mol Vis. 2008 Jun 23;14:1204-8.