Cyclic Vomiting Syndrome; Cvs
Clinical Features
Top most frequent phenotypes and symptoms related to Cyclic Vomiting Syndrome; Cvs
- Intellectual disability
- Seizures
- Global developmental delay
- Generalized hypotonia
- Hearing impairment
- Microcephaly
- Ataxia
- Growth delay
- Strabismus
- Muscle weakness
And another 28 symptoms. If you need more information about this disease we can help you.
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.
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.Cyclic Vomiting Syndrome; Cvs Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Mitochondrial Neurogastrointestinal Encephalopathy (MNGIE) Evaluation (TYMP, RRM2B, MELAS).
By Athena Diagnostics Inc (United States).
RRM2B, TYMP, MT-TL1
Specificity
34 %
Genes
100 % |
Progressive External Ophthalmoplegia Evaluation (POLG, TWINKLE, ANT1, OPA1, MELAS).
By Athena Diagnostics Inc (United States).
SLC25A4, TWNK, MT-TL1, OPA1, POLG
Specificity
20 %
Genes
100 % |
Common Mitochondrial Disorders Evaluation (POLG, MELAS, MERRF, NARP).
By Athena Diagnostics Inc (United States).
MT-TK, MT-TL1, POLG
Specificity
34 %
Genes
100 % |
MELAS mtDNA Evaluation.
By Athena Diagnostics Inc (United States).
MT-TL1
Specificity
100 %
Genes
100 % |
Juvenile myopathy, encephalopathy, lactic acidosis AND stroke.
By Center for Human Genetics, Inc (United States).
MT-TL1
Specificity
100 %
Genes
100 % |
OtoSCOPE.
By Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics (United States).
ROR1, SIX1, SIX5, SLC22A4, SNAI2, SMPX, SOX10, TBX1, TWNK, TCOF1, TECTA, TIMM8A, TJP2, TMPRSS3, USH1C, USH2A, CLRN1, TSPEAR, WFS1, ESPN , (...)
View the complete list with 130 more genes
Specificity
1 %
Genes
100 % |
Comprehensive Mitochondrial Metabolic Panel.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).
BCS1L, SCO1, SCO2, SDHB, SDHC, SDHD, SLC22A5, SLC25A13, SLC25A15, SLC25A3, SLC25A4, BTD, SUCLA2, SUCLG1, SURF1, TAZ, TWNK, TCN2, TFAM, TIMM8A , (...)
View the complete list with 173 more genes
Specificity
1 %
Genes
100 % |
Mitochondrial Genome Sequence.
By Molecular Genetics Laboratory Centro de Investigaciones Endocrinologicas "Dr. Cesar Bergada" (Argentina).
MT-CO1, MT-CO2, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, MT-ND6, MT-RNR1, MT-RNR2, MT-TA, MT-TC, MT-TD, MT-TE, MT-TF, MT-TG, MT-TH , (...)
View the complete list with 15 more genes
Specificity
3 %
Genes
100 % |
You can get up to 32 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Genetic Syndrome FinderIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J; LGMD2J OMENN SYNDROME PITT-HOPKINS SYNDROME; PTHS MACULAR DEGENERATION, AGE-RELATED, 2; ARMD2 AMELOGENESIS IMPERFECTA, TYPE IG; AI1G