A 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.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Cleft palate | MONDO:0016064 | 10 | |
| Cleft lip | MONDO:0004747 | 5 | |
| Cleft lip/palate | MONDO:0016044 | 4 | |
| Cleft lip and alveolus | MONDO:0015420 | 1 | |
| ARHGAP29-related non-syndromic orofacial cleft | MONDO:1060132 | ARHGAP29 | |
| GRHL3-related orofacial clefting | MONDO:0100579 | GRHL3 | |
| Cleft lip/palate-ectodermal dysplasia syndrome | MONDO:0009151 | NECTIN1 | |
| Familial median cleft of the upper and lower lips | MONDO:0014388 | ||
| Orofacial cleft 1 | MONDO:0007335 | ||
| Orofacial cleft 12 | MONDO:0013023 | ||
| Orofacial cleft 13 | MONDO:0013466 | ||
| Orofacial cleft 2 | MONDO:0011276 | ||
| Orofacial cleft 4 | MONDO:0012022 | ||
| Orofacial cleft 7 | MONDO:0700251 | ||
| Orofacial cleft 8 | MONDO:0029145 | TP63 | |
| Orofacial cleft 9 | MONDO:0012478 |
Rare disease
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