Disease Browser
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Parent Node: Abnormalities, Multiple (D000015) |
Parent Node: Cleft Lip (D002971) |
Parent Node: Cleft Palate (D002972) |
..Starting node ..Van der Woude syndrome 2 (C536529)
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Child Nodes:
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Sister Nodes: |
..Aase Smith syndrome (C535332)
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..Acromegaloid features, overgrowth, cleft palate, and hernia (C535656)
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..Ankyloblepharon filiforme adnatum cleft palate (C536373)
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..Aughton syndrome (C538269)
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..Baetz-Greenwalt syndrome (C537795)
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..Bamforth syndrome (C537901)
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..Baraitser Rodeck Garner syndrome (C537906)
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..Bixler Christian Gorlin syndrome (C537632)
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..Blepharo-cheilo-dontic syndrome (C536188)
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..Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies (C563414)
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..Cleft Lip with or without Cleft Palate, Nonsyndromic, 7 (C565603)
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..Cleft Palate with Ankyloglossia (C564442)
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..Cleft palate X-linked (C536426)
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..Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly (C563936)
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..Cleft Palate, Deafness, and Oligodontia (C565844)
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..Cleft Palate, Isolated, And Mental Retardation (C566991)
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..Cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss (C536427)
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..Cleft Soft Palate (C562950)
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..Coloboma of Macula and Skeletal Anomalies (C565686)
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..Coloboma, cleft lip/palate and mental retardation syndrome (C535971)
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..Coloboma, Uveal, with Cleft Lip and Palate and Mental Retardation (C565173)
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..Contractures ectodermal dysplasia cleft lip palate (C535465)
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..Craniosynostosis Mental Retardation Clefting Syndrome (C565663)
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..Crumpled helices and small mouth (C536217)
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..Diamond-Blackfan Anemia With Microtia And Cleft Palate (C565256)
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..Dyssegmental dysplasia, Rolland-Desbuquois type (C537999)
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..Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 (C565062)
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..Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 (C565799)
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..Ectrodactyly-cleft lip/palate syndrome (C536189)
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..Ectrodactyly-Cleft Palate Syndrome (C565064)
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..Emanuel syndrome (C535733)
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..Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly (C566524)
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..Faciocardiorenal syndrome (C536388)
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..Familial popliteal pterygium syndrome (C535891)
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..Feingold Trainer syndrome (C536179)
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..FRONTONASAL DYSPLASIA 3 (OMIM:613456)
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..Genito palato cardiac syndrome (C537683)
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..Gordon syndrome (C537288)
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..Halal syndrome (C535622)
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..Hardikar syndrome (C535632)
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..Hay Wells syndrome recessive type (C535846)
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..Hay-Wells syndrome (C535847)
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..Ho Kaufman Mcalister syndrome (C538325)
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..Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate (C564484)
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..Holzgreve Wagner Rehder syndrome (C535327)
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..Hydronephrosis, Congenital, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation (C565736)
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..Hypodontia Oligodontia with Orofacial Cleft (C566995)
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..Hypotrichosis, Progressive Patterned Scalp, with Wiry Hair, Onycholysis, and Cleft Lip/Palate (C563765)
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..Iida Kannari syndrome (C536284)
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..Kallmann Syndrome 2 with Cleft Lip or Palate (C563651)
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..Kapur Toriello syndrome (C537008)
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..Kniest dysplasia (C537207)
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..Kuster syndrome (C538126)
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..Ladda Zonana Ramer syndrome (C538135)
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..Larsen syndrome, dominant type (C537873)
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..Lissencephaly, Familial, with Cleft Palate and Cerebellar Hypoplasia (C565781)
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..Lowry Maclean syndrome (C537037)
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..Macrosomia with lethal microphthalmia (C537830)
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..Martinez Monasterio Pinheiro syndrome (C536027)
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..McPherson Clemens syndrome (C538160)
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..Microcephaly, corpus callosum dysgenesis and cleft lip-palate (C537547)
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..Microtia, Hearing Impairment, And Cleft Palate (C567359)
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..Multiple Epiphyseal Dysplasia with Robin Phenotype (C563291)
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..Native American myopathy (C538343)
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..Oculomaxillofacial dysostosis (C537736)
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..Oculopalatocerebral Syndrome (C564935)
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..Omphalocele cleft palate syndrome lethal (C537747)
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..Opitz GBBB Syndrome, X-Linked (C567932)
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..Orofacial Cleft 1 (C566121)
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..Orofacial Cleft 10 (C566605)
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..Orofacial Cleft 11 (C567410)
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..Orofacial Cleft 12 (C567548)
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..OROFACIAL CLEFT 13 (OMIM:613857)
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..Orofacial Cleft 2 (C566419)
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..Orofacial Cleft 3 (C563448)
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..Orofacial Cleft 4 (C564251)
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..Orofacial Cleft 5 (C563843)
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..Orofacial Cleft 8 (C565069)
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..Orofacial Cleft 9 (C563675)
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..Palant cleft palate syndrome (C538102)
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..PARC syndrome (C537174)
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..Piepkorn Karp Hickok syndrome (C535774)
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..Pilotto syndrome (C537400)
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..Popliteal Pterygium Syndrome (C562509)
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..Popliteal Pterygium Syndrome, Lethal Type (C564874)
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..Raine syndrome (C535282)
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..Rapp-Hodgkin syndrome (C535289)
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..Reardon Hall Slaney syndrome (C535294)
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..Rosselli-Gulienetti Syndrome (C563117)
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..Sakoda Complex (C567055)
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..Samson Viljoen syndrome (C537231)
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..Say syndrome (C536621)
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..Schilbach-Rott Syndrome Ocular Hypotelorism, Submucosal Cleft Palate, and Hypospadias (C563509)
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..Schrander-Stumpel Theunissen Hulsmans syndrome (C536639)
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..Seres-Santamaria Arimany Muniz syndrome (C537585)
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..Spondyloepiphyseal Dysplasia With Coronal Craniosynostosis, Cataracts, Cleft Palate, And Mental Retardation (C566515)
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..Tooth Agenesis, Selective, With Orofacial Cleft (C566994)
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..Van der Woude syndrome (C536528) 1
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..Van der Woude syndrome 2 (C536529)
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..Yim Ebbin syndrome (C536713)
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..Zadik Barak Levin syndrome (C536721)
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..Zlotogora-Ogur syndrome (C536726)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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