Details of Disease

General Information of Disease (ID: DISBI7H9)

Disease Name Cataract 39 multiple types
Synonyms
cataract 39, multiple types; early-onset non-syndromic cataract caused by mutation in CRYGB; cataract 39, multiple types, autosomal dominant; CRYGB early-onset non-syndromic cataract; autosomal dominant cataract 39 multiple types; CTRCT39
Definition Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the CRYGB gene.
Disease Hierarchy
DIS4VPS0: Early-onset non-syndromic cataract
DISBI7H9: Cataract 39 multiple types
Disease Identifiers
MONDO ID
MONDO_0014075
UMLS CUI
C3808800
OMIM ID
615188
MedGen ID
815130

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
CRYGB OTU4GEMD Limited Autosomal dominant [1]
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References

1 Polymorphisms of the gamma crystallin A and B genes among Indian patients with pediatric cataract. J Postgrad Med. 2011 Jul-Sep;57(3):201-5. doi: 10.4103/0022-3859.85205.