Cranioectodermal dysplasia type 1

Summary: Cranioectodermal dysplasia is a disorder that affects many parts of the body. The most common features involve bone abnormalities and abnormal development of certain tissues known as ectodermal tissues, which include the skin, hair, nails, and teeth. The signs ...1

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Symptoms of Cranioectodermal dysplasia type 1

Clinical features: Imported from Human Phenotype Ontology (HPO)

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Genetics of Cranioectodermal dysplasia type 1

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

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Names and Terminology

Synonyms: Cranioectodermal Dysplasia ; LEVIN SYNDROME I ; Levin syndrome 1 ...Source: GTR (NCBI/NIH)3 ...

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References

  1. Source: GTR (NCBI/NIH): ncbi.nlm.nih.gov/ gtr/ conditions/ C0432235/ 
  2. ibid.
  3. ibid.

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