Cranioectodermal dysplasia type 2

Cranioectodermal dysplasia type 2: See http://www.omim.org/entry/613610 ...1

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Symptoms of Cranioectodermal dysplasia type 2

Clinical features: Imported from Human Phenotype Ontology (HPO)

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Genetics of Cranioectodermal dysplasia type 2

Modes of inheritance: Autosomal recessive inheritance (HPO, OMIM, Orphanet) ...Source: GTR (NCBI/NIH)2 ...

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Names and Terminology

Synonyms: Cranioectodermal Dysplasia ...Source: GTR (NCBI/NIH)3 ...

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References

  1. Source: Monarch Initiative
  2. Source: GTR (NCBI/NIH): ncbi.nlm.nih.gov/ gtr/ conditions/ C3150874/ 
  3. ibid.

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