Michels syndrome

Symptoms of Michels syndrome

Clinical features: Imported from Human Phenotype Ontology (HPO)

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Genetics of Michels syndrome

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

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Names and Terminology

Synonyms: 3MC SYNDROME 1 ; Craniosynostosis with lid anomalies ; Oculopalatoskeletal syndrome ...Source: GTR (NCBI/NIH)2 ...

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References

  1. Source: GTR (NCBI/NIH): ncbi.nlm.nih.gov/ gtr/ conditions/ C0796059/ 
  2. ibid.

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