| Disease Browser
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Parent Node:
 Jaw Abnormalities (D007569) |
Parent Node:
Mouth Abnormalities (D009056) |
..Starting node
.. Cleft Palate (D002972)
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Child Nodes:
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| ........Aase Smith syndrome (C535332) |
| ........Acromegaloid features, overgrowth, cleft palate, and hernia (C535656) |
| ........Ankyloblepharon filiforme adnatum cleft palate (C536373) |
| ........Aughton syndrome (C538269) |
| ........Baetz-Greenwalt syndrome (C537795) |
| ........Bamforth syndrome (C537901) |
| ........Baraitser Rodeck Garner syndrome (C537906) |
| ........Bixler Christian Gorlin syndrome (C537632) |
| ........Blepharo-cheilo-dontic syndrome (C536188) |
| ........Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies (C563414) |
| ........Cleft Lip with or without Cleft Palate, Nonsyndromic, 7 (C565603) |
| ........Cleft Palate with Ankyloglossia (C564442) |
| ........Cleft palate X-linked (C536426) |
| ........Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly (C563936) |
| ........Cleft Palate, Deafness, and Oligodontia (C565844) |
| ........Cleft Palate, Isolated, And Mental Retardation (C566991) |
| ........Cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss (C536427) |
| ........Cleft Soft Palate (C562950) |
| ........Coloboma of Macula and Skeletal Anomalies (C565686) |
| ........Coloboma, cleft lip/palate and mental retardation syndrome (C535971) |
| ........Coloboma, Uveal, with Cleft Lip and Palate and Mental Retardation (C565173) |
| ........Contractures ectodermal dysplasia cleft lip palate (C535465) |
| ........Craniosynostosis Mental Retardation Clefting Syndrome (C565663) |
| ........Crumpled helices and small mouth (C536217) |
| ........Diamond-Blackfan Anemia With Microtia And Cleft Palate (C565256) |
| ........Dyssegmental dysplasia, Rolland-Desbuquois type (C537999) |
| ........Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 (C565062) |
| ........Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 (C565799) |
| ........Ectrodactyly-cleft lip/palate syndrome (C536189) |
| ........Ectrodactyly-Cleft Palate Syndrome (C565064) |
| ........Emanuel syndrome (C535733) |
| ........Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly (C566524) |
| ........Faciocardiorenal syndrome (C536388) |
| ........Familial popliteal pterygium syndrome (C535891) |
| ........Feingold Trainer syndrome (C536179) |
| ........FRONTONASAL DYSPLASIA 3 (OMIM:613456) |
| ........Genito palato cardiac syndrome (C537683) |
| ........Gordon syndrome (C537288) |
| ........Halal syndrome (C535622) |
| ........Hardikar syndrome (C535632) |
| ........Hay Wells syndrome recessive type (C535846) |
| ........Hay-Wells syndrome (C535847) |
| ........Ho Kaufman Mcalister syndrome (C538325) |
| ........Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate (C564484) |
| ........Holzgreve Wagner Rehder syndrome (C535327) |
| ........Hydronephrosis, Congenital, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation (C565736) |
| ........Hypodontia Oligodontia with Orofacial Cleft (C566995) |
| ........Hypotrichosis, Progressive Patterned Scalp, with Wiry Hair, Onycholysis, and Cleft Lip/Palate (C563765) |
| ........Iida Kannari syndrome (C536284) |
| ........Kallmann Syndrome 2 with Cleft Lip or Palate (C563651) |
| ........Kapur Toriello syndrome (C537008) |
| ........Kniest dysplasia (C537207) |
| ........Kuster syndrome (C538126) |
| ........Ladda Zonana Ramer syndrome (C538135) |
| ........Larsen syndrome, dominant type (C537873) |
| ........Lissencephaly, Familial, with Cleft Palate and Cerebellar Hypoplasia (C565781) |
| ........Lowry Maclean syndrome (C537037) |
| ........Macrosomia with lethal microphthalmia (C537830) |
| ........Martinez Monasterio Pinheiro syndrome (C536027) |
| ........McPherson Clemens syndrome (C538160) |
| ........Microcephaly, corpus callosum dysgenesis and cleft lip-palate (C537547) |
| ........Microtia, Hearing Impairment, And Cleft Palate (C567359) |
| ........Multiple Epiphyseal Dysplasia with Robin Phenotype (C563291) |
| ........Native American myopathy (C538343) |
| ........Oculomaxillofacial dysostosis (C537736) |
| ........Oculopalatocerebral Syndrome (C564935) |
| ........Omphalocele cleft palate syndrome lethal (C537747) |
| ........Opitz GBBB Syndrome, X-Linked (C567932) |
| ........Orofacial Cleft 1 (C566121) |
| ........Orofacial Cleft 10 (C566605) |
| ........Orofacial Cleft 11 (C567410) |
| ........Orofacial Cleft 12 (C567548) |
| ........OROFACIAL CLEFT 13 (OMIM:613857) |
| ........Orofacial Cleft 2 (C566419) |
| ........Orofacial Cleft 3 (C563448) |
| ........Orofacial Cleft 4 (C564251) |
| ........Orofacial Cleft 5 (C563843) |
| ........Orofacial Cleft 8 (C565069) |
| ........Orofacial Cleft 9 (C563675) |
| ........Palant cleft palate syndrome (C538102) |
| ........PARC syndrome (C537174) |
| ........Piepkorn Karp Hickok syndrome (C535774) |
| ........Pilotto syndrome (C537400) |
| ........Popliteal Pterygium Syndrome (C562509) |
| ........Popliteal Pterygium Syndrome, Lethal Type (C564874) |
| ........Raine syndrome (C535282) |
| ........Rapp-Hodgkin syndrome (C535289) |
| ........Reardon Hall Slaney syndrome (C535294) |
| ........Rosselli-Gulienetti Syndrome (C563117) |
| ........Sakoda Complex (C567055) |
| ........Samson Viljoen syndrome (C537231) |
| ........Say syndrome (C536621) |
| ........Schilbach-Rott Syndrome Ocular Hypotelorism, Submucosal Cleft Palate, and Hypospadias (C563509) |
| ........Schrander-Stumpel Theunissen Hulsmans syndrome (C536639) |
| ........Seres-Santamaria Arimany Muniz syndrome (C537585) |
| ........Spondyloepiphyseal Dysplasia With Coronal Craniosynostosis, Cataracts, Cleft Palate, And Mental Retardation (C566515) |
| ........Tooth Agenesis, Selective, With Orofacial Cleft (C566994) |
........Van der Woude syndrome (C536528)  1 |
| ........Van der Woude syndrome 2 (C536529) |
| ........Yim Ebbin syndrome (C536713) |
| ........Zadik Barak Levin syndrome (C536721) |
| ........Zlotogora-Ogur syndrome (C536726) |
Sister Nodes: |
..Ankyloglossia (C562396)
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..Calabro syndrome (C537960)
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..Cleft Lip (D002971) 59
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..Cleft Palate (D002972) 103
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..Cleft Palate-Lateral Synechia Syndrome (C563047)
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..Contractures, Congenital, Torticollis, and Malignant Hyperthermia (C565679)
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..Fibromatosis, Gingival (D005351) 11
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..Jagell Holmgren Hofer syndrome (C537364)
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..Macrostomia (D008265) 3
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..Microstomia (D008865) 4
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..Taurodontism, microdontia, and dens invaginatus (C536947)
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..Temtamy preaxial brachydactyly syndrome (C536958)
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..Velopharyngeal Insufficiency (D014681)
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..Verloove-Vanhorick Brubakk syndrome (C536541)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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