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 PSEUDOHYPOPARATHYROIDISM, TYPE IB; PHP1B MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT EPILEPSY, NOCTURNAL FRONTAL LOBE, 4; ENFL4 DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT; DYT4 B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY; BENTA SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W; LGMD2W