Disease Browser
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Parent Node: Cleft Lip (D002971) |
..Starting node ..Cleft Lip, Congenital Healed (C563468)
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Child Nodes:
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Sister Nodes: |
..Ankyloblepharon filiforme adnatum cleft palate (C536373)
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..Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects (C566351)
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..Ausems Wittebol-Post Hennekam syndrome (C538272)
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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 Lip with or without Cleft Palate, Nonsyndromic, 8 (C565070)
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..Cleft Lip, Congenital Healed (C563468)
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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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..Craniosynostosis Mental Retardation Clefting Syndrome (C565663)
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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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..Familial popliteal pterygium syndrome (C535891)
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..Hay Wells syndrome recessive type (C535846)
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..Hay-Wells syndrome (C535847)
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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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..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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..Kallmann Syndrome 2 with Cleft Lip or Palate (C563651)
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..Kapur Toriello syndrome (C537008)
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..Krause-Kivlin syndrome (C537617)
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..Kuster syndrome (C538126)
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..Larsen syndrome, dominant type (C537873)
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..Martinez Monasterio Pinheiro syndrome (C536027)
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..McPherson Clemens syndrome (C538160)
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..Median cleft lip, corpus callosum, lipoma, and skin polyps (C536135)
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..Microcephaly, corpus callosum dysgenesis and cleft lip-palate (C537547)
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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 6, SUSCEPTIBILITY TO (OMIM:608864)
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..Orofacial Cleft 7 (C563464)
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..Orofacial Cleft 8 (C565069)
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..Orofacial Cleft 9 (C563675)
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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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..Rapp-Hodgkin syndrome (C535289)
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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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..Short Stature, Mental Retardation, Callosal Agenesis, Heminasal Hypoplasia, Microphthalmia, And Atypical Clefting (C566989)
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..Thomas syndrome (C536514)
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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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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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