1. Mendelian
  2. Rare Diseases
  3. SECKEL SYNDROME 10; SCKL10

Seckel Syndrome 10; Sckl10

Table of contents:

Genes related to Seckel Syndrome 10; Sckl10

  • NSMCE2

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Seckel Syndrome 10; Sckl10

  • Short stature
  • Microcephaly
  • Micrognathia
  • Abnormal facial shape
  • Hypertension
  • Congestive heart failure
  • Dilatation
  • Severe short stature
  • Diabetes mellitus
  • Hepatic steatosis

And another 19 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.

Seckel Syndrome 10; Sckl10 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
NSMCE2.

By Fulgent Genetics Fulgent Genetics (United States).

NSMCE2
Specificity
100 %
Genes
100 %

You can get up to -7 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Search Engine

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