Short Stature, Rhizomelic, With Microcephaly, Micrognathia, And Developmental Delay; Srmmd
Table of contents:
Genes related to Short Stature, Rhizomelic, With Microcephaly, Micrognathia, And Developmental Delay; Srmmd
- ARCN1
Clinical Features
Top most frequent phenotypes and symptoms related to Short Stature, Rhizomelic, With Microcephaly, Micrognathia, And Developmental Delay; Srmmd
- Intellectual disability
- Seizures
- Global developmental delay
- Short stature
- Microcephaly
- Failure to thrive
- Micrognathia
- Cleft palate
- Cataract
- Cryptorchidism
And another 22 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.Short Stature, Rhizomelic, With Microcephaly, Micrognathia, And Developmental Delay; Srmmd Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
ARCN1.
By Fulgent Genetics Fulgent Genetics (United States).
ARCN1
Specificity
100 %
Genes
100 % |
You can get up to -7 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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