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Children's Health

Medical Reference Related to Children's Health

  1. Oral-Facial-Digital Syndrome

    Important It is possible that the main title of the report Oral Facial Digital Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

  2. Acrocallosal Syndrome, Schinzel Type

    Important It is possible that the main title of the report Acrocallosal Syndrome, Schinzel Type is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

  3. WAGR Syndrome/11p Deletion Syndrome

    Important It is possible that the main title of the report WAGR Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

  4. Autosomal Recessive Hyper IgE Syndrome

    Important It is possible that the main title of the report Job Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

  5. Hyperekplexia

    Important It is possible that the main title of the report Hyperexplexia is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

  6. Marcus Gunn Phenomenon

    Important It is possible that the main title of the report Marcus Gunn Phenomenon is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

  7. Chromosome 11, Partial Monosomy 11q

    Important It is possible that the main title of the report Chromosome 11, Partial Monosomy 11q is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

  8. X-Linked Myopathy with Excessive Autophagy

    X-linked myopathy with excessive autophagy (XMEA) is an extremely rare genetic disorder characterized by muscle disease (myopathy). The disorder is fully expressed in males only and is characterized by slowly progressive muscle weakness,especially in the legs. Onset is usually during childhood often between 5-10 years of age. XMEA occurs due to mutations of an unidentified gene on the X ...

  9. Klippel-Feil Syndrome

    Important It is possible that the main title of the report Klippel - Feil Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

  10. Meningococcemia

    Important It is possible that the main title of the report Meningococcemia is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

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