Alazami-yuan Syndrome; Alyus

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Alazami-yuan Syndrome; Alyus

TAF6

View recommended genes panels

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.

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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 Panel complete gene list SMARCA4, SMARCB1, SMARCE1, ARID1A, SMC1A, SOX11, TAF1, TAF6, MED12, HDAC8, CTCF, SRCAP, AFF4, ARID1B, PHF6, DOCK6, CHD7, WDR26, ANKRD11, CREBBP, SMC3, ESCO2, EOGT, NIPBL, KDM1A, DLL4, ARHGAP31, EP300, RBPJ, NOTCH1, RAD21 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 %

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

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