Microcephaly 19, Primary, Autosomal Recessive; Mcph19

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

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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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