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.

Click here to know more about Mendelian.

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 more

Sources and references

You can check the following sources for additional information.

OMIM Genetic Syndrome Finder

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2; MPPH2 PITUITARY APOPLEXY GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF GLOMUVENOUS MALFORMATIONS; GVM AICARDI-GOUTIERES SYNDROME 7; AGS7 TSH-SECRETING PITUITARY ADENOMA