Orofacial cleft
MONDO:0000358A disorder of facial skeleton that is characterized by cleft lip and/or cleft palate that result in feeding, speech and hearing problems caused by failures during development.
70 clinical trials for this condition and its sub-types, 4 tagged with Orofacial cleft itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Orofacial cleft
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Cleft palate 34 trials · 35 incl. sub-types
9 sub-types
- Isolated cleft palate 3 trials Sub-types →
- Submucosal cleft palate 1 trial
- Kuster syndrome 0 trials
- Rapp-Hodgkin syndrome 0 trials
- Bifid uvula 0 trials
- Cleft hard palate 0 trials
- Cleft palate with or without ankyloglossia, X-linked 0 trials
- Cleft soft palate 0 trials
- Soft and hard cleft palate 0 trials
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Cleft lip 31 trials
3 sub-types
- Kuster syndrome 0 trials
- Rapp-Hodgkin syndrome 0 trials
- Isolated cleft lip 0 trials Sub-types →
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Cleft lip/palate 31 trials
4 sub-types
- Orofacial cleft 10 0 trials
- Orofacial cleft 11 0 trials
- Orofacial cleft 15 0 trials
- Orofacial cleft 5 0 trials
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Cleft lip and alveolus 17 trials
1 sub-type
- Orofacial cleft 5 0 trials
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Orofacial cleft 1 1 trial
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GRHL3-related orofacial clefting 0 trials
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Orofacial cleft 12 0 trials
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Orofacial cleft 13 0 trials
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Orofacial cleft 2 0 trials
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Orofacial cleft 4 0 trials
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Orofacial cleft 7 0 trials
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Orofacial cleft 8 0 trials
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Orofacial cleft 9 0 trials