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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Congenital Abnormalities [MESH:D000013] > Stomatognathic System Abnormalities [MESH:D018640] > Mouth Abnormalities [MESH:D009056] > Cleft Lip [MESH:D002971]
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The current query selects 914 items in 56 groups, which could be too many to show at once. If you are sure you want to see them all, you can proceed to see the entire category, 'or select a more specific subcategory of "Cleft Lip [MESH:D002971]" below.

Subcategories in C16. Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesCongenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Congenital Abnormalities [MESH:D000013] > Stomatognathic System Abnormalities [MESH:D018640] > Mouth Abnormalities [MESH:D009056] > Cleft Lip [MESH:D002971]:
(jump to A - B - C - E - F - H - K - L - M - O - P - R - S - T - V - Y)
- A -
Ankyloblepharon filiforme adnatum cleft palate [MESH:C536373] (1)
Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects [MESH:C566351] (1)
Ausems Wittebol-Post Hennekam syndrome [MESH:C538272] (1)
 
- B -
Baraitser Rodeck Garner syndrome [MESH:C537906] (1)
Bixler Christian Gorlin syndrome [MESH:C537632] (1)
Blepharo-cheilo-dontic syndrome [MESH:C536188] (1)
 
- C -
Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies [MESH:C563414] (1)
Cleft Lip with or without Cleft Palate, Nonsyndromic, 7 [MESH:C565603] (1)
Cleft Lip with or without Cleft Palate, Nonsyndromic, 8 [MESH:C565070] (1)
Cleft Lip, Congenital Healed [MESH:C563468] (1)
Coloboma, Uveal, with Cleft Lip and Palate and Mental Retardation [MESH:C565173] (1)
Coloboma, cleft lip/palate and mental retardation syndrome [MESH:C535971] (1)
Craniosynostosis Mental Retardation Clefting Syndrome [MESH:C565663] (1)
 
- E -
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 [MESH:C565062] (1)
Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)
Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)
 
- F -
Familial popliteal pterygium syndrome [MESH:C535891] (1)
 
- H -
Hay Wells syndrome recessive type [MESH:C535846] (1)
Hay-Wells syndrome [MESH:C535847] (46)
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate [MESH:C564484] (1)
Holzgreve Wagner Rehder syndrome [MESH:C535327] (1)
Hypodontia Oligodontia with Orofacial Cleft [MESH:C566995] (1)
Hypotrichosis, Progressive Patterned Scalp, with Wiry Hair, Onycholysis, and Cleft Lip/Palate [MESH:C563765] (1)
 
- K -
Kallmann Syndrome 2 with Cleft Lip or Palate [MESH:C563651] (1)
Kapur Toriello syndrome [MESH:C537008] (1)
Krause-Kivlin syndrome [MESH:C537617] (5)
Kuster syndrome [MESH:C538126] (1)
 
- L -
Larsen syndrome, dominant type [MESH:C537873] (44)
 
- M -
Martinez Monasterio Pinheiro syndrome [MESH:C536027] (1)
McPherson Clemens syndrome [MESH:C538160] (1)
Median cleft lip, corpus callosum, lipoma, and skin polyps [MESH:C536135] (1)
Microcephaly, corpus callosum dysgenesis and cleft lip-palate [MESH:C537547] (1)
 
- O -
Orofacial Cleft 1 [MESH:C566121] (81)
Orofacial Cleft 10 [MESH:C566605] (39)
Orofacial Cleft 11 [MESH:C567410] (101)
Orofacial Cleft 12 [MESH:C567548] (1)
Orofacial Cleft 2 [MESH:C566419] (1)
Orofacial Cleft 3 [MESH:C563448] (1)
Orofacial Cleft 4 [MESH:C564251] (1)
Orofacial Cleft 5 [MESH:C563843] (38)
Orofacial Cleft 7 [MESH:C563464] (1)
Orofacial Cleft 8 [MESH:C565069] (1)
Orofacial Cleft 9 [MESH:C563675] (1)
 
- P -
Pilotto syndrome [MESH:C537400] (1)
Popliteal Pterygium Syndrome [MESH:C562509] (33)
Popliteal Pterygium Syndrome, Lethal Type [MESH:C564874] (1)
 
- R -
Rapp-Hodgkin syndrome [MESH:C535289] (46)
Rosselli-Gulienetti Syndrome [MESH:C563117] (25)
 
- S -
Sakoda Complex [MESH:C567055] (1)
Samson Viljoen syndrome [MESH:C537231] (1)
Short Stature, Mental Retardation, Callosal Agenesis, Heminasal Hypoplasia, Microphthalmia, And Atypical Clefting [MESH:C566989] (1)
 
- T -
Thomas syndrome [MESH:C536514] (1)
Tooth Agenesis, Selective, With Orofacial Cleft [MESH:C566994] (1)
 
- V -
Van der Woude syndrome 2 [MESH:C536529] (1)
Van der Woude syndrome [MESH:C536528] (33)
 
- Y -
Yim Ebbin syndrome [MESH:C536713] (1)