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Acephalostomia

MedGen UID:
672818
Concept ID:
C0685897
Congenital Abnormality
SNOMED CT: Acephalostomia (91849001)

Definition

A congenital defect characterized by the absence of most or all of the head, with the presence of a mouth-like opening on the upper thorax. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVAcephalostomia

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