Alazami-yuan Syndrome; Alyus
Clinical Features
Top most frequent phenotypes and symptoms related to Alazami-yuan Syndrome; Alyus
- Intellectual disability
- Global developmental delay
- Short stature
- Generalized hypotonia
- Microcephaly
- Strabismus
- Abnormal facial shape
- Cryptorchidism
- High palate
- Feeding difficulties
And another 24 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.Alazami-yuan Syndrome; Alyus Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Cornelia de Lange Syndrome and Cornelia de Lange Syndrome-Related Disorders Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
SMARCA4, SMARCB1, SMARCE1, ARID1A, SMC1A, SOX11, TAF1, TAF6, MED12, HDAC8, CTCF, SRCAP, AFF4, ARID1B, PHF6, DOCK6, CHD7, WDR26, ANKRD11, CREBBP , (...)
View the complete list with 11 more genes
Specificity
4 %
Genes
100 % |
Cornelia de Lange Syndrome.
By Asper Biogene Asper Biogene LLC (Estonia).
SMC1A, TAF6, HDAC8, AFF4, ANKRD11, SMC3, NIPBL, RAD21
Specificity
13 %
Genes
100 % |
TAF6.
By Fulgent Genetics Fulgent Genetics (United States).
TAF6
Specificity
100 %
Genes
100 % |
You can get up to -5 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 RENAL CYSTS AND DIABETES SYNDROME; RCAD MYOPATHY, CENTRONUCLEAR, 1; CNM1 GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET; IMNEPD APERT SYNDROME DEAFNESS, AUTOSOMAL RECESSIVE 44; DFNB44 MYASTHENIC SYNDROME, CONGENITAL, 17; CMS17