Facial cleft

MONDO:0015411

A 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

3 clinical trials for this condition and its sub-types, 0 tagged with Facial cleft itself.

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Where it sits in the disease tree

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Part of

↑ Developmental defect during embryogenesis (1060) ↑ Disorder of facial skeleton (132)

Sub-types of Facial cleft

Commissural facial cleft 1 trial
Bifid nose 0 trials · 1 incl. sub-types
3 sub-types
- BNAR syndrome 1 trial
- Bifid nose, autosomal dominant 0 trials
- Bifid nose, autosomal recessive 0 trials Sub-types →
Tessier number 5 facial cleft 0 trials
Tessier number 6 facial cleft 0 trials
Coloboma of inferior eyelid 0 trials
Coloboma of superior eyelid 0 trials
Median cleft lip/mandibule 0 trials
Median cleft of the upper lip and maxilla 0 trials
Midline cervical cleft 0 trials

Most studied deeper sub-types

Paramedian nasal cleft (0)

Including sub-types (3) Tagged with Facial cleft (0)

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