EEM syndrome

Symptoms of EEM syndrome

Symptoms: The Human Phenotype Ontology (HPO) provides the following list of features that have been reported in people with this condition. Much of the information in the HPO comes from Orphanet, a European rare disease database. Signs and Symptoms

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Genetics of EEM syndrome

Modes of inheritance: Autosomal recessive inheritance (HPO, OMIM, Orphanet) ...Source: GTR (NCBI/NIH)1 ...

... More on Genetics of EEM syndrome »

Names and Terminology

Other Names: Ectodermal dysplasia, ectrodactyly, and macular dystrophy ...Source: GARD (NIH)2 ...

... More General Information on EEM syndrome »

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References

  1. Source: GTR (NCBI/NIH): ncbi.nlm.nih.gov/ gtr/ conditions/ C1857041/ 
  2. Source: GARD (NIH): rarediseases.info.nih.gov/ diseases/ 2078/ eem-syndrome

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Note: This site is for informational purposes only and is not medical advice. See your doctor or other qualified medical professional for all your medical needs.