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Polyrrhinia

MedGen UID:
894825
Concept ID:
C4274730
Congenital Abnormality
Synonyms: Congenital duplication of nose; Double nose; Polyrhinia; polyrrhinia
SNOMED CT: Congenital duplication of nose (716279002); Polyrrhinia (716279002); Double nose (716279002)
Modes of inheritance:
Not genetically inherited
MedGen UID:
988794
Concept ID:
CN307044
Finding
Source: Orphanet
clinical entity without genetic inheritance.
 
Monarch Initiative: MONDO:0015388
Orphanet: ORPHA141091

Definition

Polyrrhinia is an extremely rare, major congenital malformation with characteristic of complete duplication of the nose resulting in two fully developed noses often associated with choanal atresia, causing respiratory distress and necessitating surgical repair. [from SNOMEDCT_US]

Term Hierarchy

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

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