Cataract 46, Juvenile-onset; Ctrct46
Table of contents:
Clinical Features
Phenotypes and symptoms related to Cataract 46, Juvenile-onset; Ctrct46
- Cleft palate
- Cataract
- Scarring
- Congenital cataract
- Aniridia
- Juvenile cataract
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Alternative names
Cataract 46, Juvenile-onset; Ctrct46 Is also known as cataract, juvenile, hutterite type.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Cataract 46, Juvenile-onset; Ctrct46 Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
Cataract panel.
By Centogene AG - the Rare Disease Company (Germany).
BFSP1, BFSP2, VIM, WFS1, UNC45B, FYCO1, CHMP4B, P3H2, VSX2, BCOR, LEMD2, AGK, SLC16A12, SIPA1L3, CRYAA, CRYAB, CRYBA1, CRYBA2, CRYBA4, CRYBB1 , (...)
View the complete list with 25 more genes
Specificity
3 %
Genes
100 % |
LEMD2.
By Fulgent Genetics Fulgent Genetics (United States).
LEMD2
Specificity
100 %
Genes
100 % |
You can get up to -6 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM MESH Genetic Syndrome FinderIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY; VRNI NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1 CLEIDOCRANIAL DYSPLASIA; CCD MICROPHTHALMIA, SYNDROMIC 12; MCOPS12 DEAFNESS, AUTOSOMAL DOMINANT 17; DFNA17
Cataract panel.
LEMD2.