Microcephaly 19, Primary, Autosomal Recessive; Mcph19
Table of contents:
Genes related to Microcephaly 19, Primary, Autosomal Recessive; Mcph19
- COPB2
Clinical Features
Top most frequent phenotypes and symptoms related to Microcephaly 19, Primary, Autosomal Recessive; Mcph19
- Global developmental delay
- Microcephaly
- Failure to thrive
- Spasticity
- Ventriculomegaly
- Hypoplasia of the corpus callosum
- Blindness
- Delayed myelination
- Decreased body weight
- Cerebral visual impairment
And another 1 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.Microcephaly 19, Primary, Autosomal Recessive; Mcph19 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
COPB2.
By Fulgent Genetics Fulgent Genetics (United States).
COPB2
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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