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Rhinocephaly

MedGen UID:
672816
•Concept ID:
C0685895
•
Congenital Abnormality
SNOMED CT: Rhinocephaly (95241002)

Definition

A congenital anatomic defect characterised by the presence of a proboscis-like nose located above the eyes, which are partially or completely fused. [from NCI]

Term Hierarchy

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

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