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Prosoposchisis

MedGen UID:: 897543
•Concept ID:: C4085564
•: Congenital Abnormality

Definition

A congenital anatomic defect characterised by a facial cleft that extends from the mouth to the orbit of the eye. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVProsoposchisis

Phenotypic abnormality
- Abnormality of prenatal development or birth
  - Fetal anomaly
    - Prosoposchisis

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Prosoposchisis
Prosoposchisis

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