Facial cleft
MONDO:0015411A congenital abnormality consisting of an opening or gap in the face, which results from incomplete fusion of one or more of the embryonic facial prominences.
Also known as: cleft face, craniofacial cleft, prosoposchisis
42 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
BNAR syndrome
(1)
Commissural facial cleft
(1)
Bifid nose
(0)
Bifid nose, autosomal dominant
(0)
Bifid nose, autosomal recessive
(0)
Coloboma of inferior eyelid
(0)
Coloboma of superior eyelid
(0)
Median cleft lip/mandibule
(0)
Median cleft of the upper lip and maxilla
(0)
Midline cervical cleft
(0)
Paramedian nasal cleft
(0)
Tessier number 5 facial cleft
(0)
Tessier number 6 facial cleft
(0)
Broader categories
Disease
(618)
Musculoskeletal system disorder
(196)
Bone disorder
(47)
Human disease
(14)
Developmental defect during embryogenesis
(7)
Disorder of facial skeleton
(4)
Skeletal system disorder
(4)
Skull disorder
(1)
Disease by body system or component
(0)
Disease by developmental or physiological process
(0)