ONTOLOGY REPORT - ANNOTATIONS


Term:cleft palate
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Accession:DOID:674 term browser browse the term
Definition:Congenital fissure of the soft and/or hard palate, due to faulty fusion.
Synonyms:exact_synonym: CP;   CPI;   cleft palates;   palatoschisis;   uranostaphyloschisis
 narrow_synonym: NONSYNDROMIC CLEFT PALATE
 primary_id: MESH:D002972
 alt_id: OMIM:119540;   RDO:0000280
For additional species annotation, visit the Alliance of Genome Resources.


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cleft palate term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Bhmt2 betaine-homocysteine S-methyltransferase 2 JBrowse link 2 23,272,320 23,289,266 RGD:11554173
G Bnc2 basonuclin 2 JBrowse link 5 102,407,508 102,807,389 RGD:11554173
G Cask calcium/calmodulin dependent serine protein kinase JBrowse link X 9,815,652 10,156,155 RGD:11554173
RGD:11576291
G Cbfb core-binding factor subunit beta JBrowse link 19 37,127,508 37,171,075 RGD:11554173
G Chuk component of inhibitor of nuclear factor kappa B kinase complex JBrowse link 1 263,848,829 263,884,354 RGD:11554173
G Col11a2 collagen type XI alpha 2 chain JBrowse link 20 3,829,324 3,859,022 RGD:12436724
RGD:12904711
G Col2a1 collagen type II alpha 1 chain JBrowse link 7 139,454,945 139,484,403 RGD:11554173
RGD:12436724
G Dlg1 discs large MAGUK scaffold protein 1 JBrowse link 11 72,164,566 72,378,895 RGD:11554173
G Dnah11 dynein, axonemal, heavy chain 11 JBrowse link 6 145,784,893 146,099,212 RGD:8554872
G Egf epidermal growth factor JBrowse link 2 68,820,616 68,895,537 RGD:11554173
G Fgf10 fibroblast growth factor 10 JBrowse link 2 51,673,480 51,747,533 RGD:11554173
G Fgf2 fibroblast growth factor 2 JBrowse link 2 124,081,072 124,134,133 RGD:11554173
G Fgf3 fibroblast growth factor 3 JBrowse link 1 218,003,018 218,006,942 RGD:11554173
G Fgf7 fibroblast growth factor 7 JBrowse link 3 118,315,859 118,368,464 RGD:11554173
G Fgf8 fibroblast growth factor 8 JBrowse link 1 265,492,949 265,498,965 RGD:11554173
G Fgf9 fibroblast growth factor 9 JBrowse link 15 38,341,657 38,386,945 RGD:11554173
G Fgfr1 Fibroblast growth factor receptor 1 JBrowse link 16 71,265,390 71,319,046 RGD:11554173
G Fgfr2 fibroblast growth factor receptor 2 JBrowse link 1 200,590,951 200,696,946 RGD:11554173
G Fgfr3 fibroblast growth factor receptor 3 JBrowse link 14 82,272,322 82,287,739 RGD:11554173
G Flna filamin A JBrowse link X 156,460,785 156,487,245 RGD:8554872
G Flnb filamin B JBrowse link 15 18,750,152 18,883,019 RGD:12791026
G Fzd4 frizzled class receptor 4 JBrowse link 1 153,589,471 153,598,376 RGD:11554173
G Gata6 GATA binding protein 6 JBrowse link 18 2,415,821 2,447,087 RGD:13208933
G Gdf6 growth differentiation factor 6 JBrowse link 5 23,056,345 23,072,666 RGD:12798509
G Gli3 GLI family zinc finger 3 JBrowse link 17 52,294,942 52,569,036 RGD:12738224
G Gnb1 G protein subunit beta 1 JBrowse link 5 172,914,025 172,981,403 RGD:8554872
G Golgb1 golgin B1 JBrowse link 11 66,761,646 66,819,115 RGD:13592920
G Grhl3 grainyhead-like transcription factor 3 JBrowse link 5 153,893,039 153,925,045 RGD:8554872
G Irf6 interferon regulatory factor 6 JBrowse link 13 111,870,121 111,889,328 RGD:1600214
RGD:12436724
RGD:8554872
RGD:11554173
G Kif7 kinesin family member 7 JBrowse link 1 141,434,183 141,452,592 RGD:11554173
G Mnt MAX network transcriptional repressor JBrowse link 10 61,683,776 61,700,504 RGD:11554173
G Msx1 msh homeobox 1 JBrowse link 14 77,712,262 77,716,061 RGD:5132609
RGD:11554173
G Mthfd1 methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1 JBrowse link 6 99,282,850 99,350,367 RGD:12914151
G Mthfs methenyltetrahydrofolate synthetase JBrowse link 8 96,564,877 96,614,386 RGD:11554173
G Mtr 5-methyltetrahydrofolate-homocysteine methyltransferase JBrowse link 17 66,210,444 66,295,014 RGD:11554173
G Myc MYC proto-oncogene, bHLH transcription factor JBrowse link 7 102,586,313 102,591,240 RGD:11554173
G Nectin1 nectin cell adhesion molecule 1 JBrowse link 8 48,094,233 48,198,499 RGD:1599795
G Nedd4l neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase JBrowse link 18 60,392,376 60,719,720 RGD:11554173
G Nfia nuclear factor I/A JBrowse link 5 116,421,895 116,750,381 RGD:8554872
G Nos3 nitric oxide synthase 3 JBrowse link 4 7,321,908 7,342,404 RGD:11554173
G Pax9 paired box 9 JBrowse link 6 77,607,705 77,624,453 RGD:12801424
G Pdgfra platelet derived growth factor receptor alpha JBrowse link 14 35,527,926 35,581,130 RGD:11554173
RGD:8554872
G Pitx2 paired-like homeodomain 2 JBrowse link 2 233,602,732 233,621,059 RGD:12910559
G Ptch1 patched 1 JBrowse link 17 1,032,242 1,085,885 RGD:11554173
G Rarg retinoic acid receptor, gamma JBrowse link 7 143,840,739 143,863,206 RGD:11554173
G Ror2 receptor tyrosine kinase-like orphan receptor 2 JBrowse link 17 11,953,552 12,134,386 RGD:11535950
G Ryk receptor-like tyrosine kinase JBrowse link 8 111,326,339 111,398,640 RGD:11554173
G Satb2 SATB homeobox 2 JBrowse link 9 63,456,877 63,642,193 RGD:11554173
RGD:8554872
G Sdc2 syndecan 2 JBrowse link 7 71,572,731 71,686,139 RGD:12798509
G Shh sonic hedgehog signaling molecule JBrowse link 4 718,538 727,691 RGD:12801424
G Shox2 short stature homeobox 2 JBrowse link 2 164,118,175 164,126,783 RGD:12859081
G Sim2 SIM bHLH transcription factor 2 JBrowse link 11 34,315,739 34,355,183 RGD:11554173
G Slc19a1 solute carrier family 19 member 1 JBrowse link 20 12,334,675 12,354,517 RGD:11554173
G Spry2 sprouty RTK signaling antagonist 2 JBrowse link 15 90,172,769 90,177,823 RGD:11554173
G Sumo1 small ubiquitin-like modifier 1 JBrowse link 9 66,453,428 66,483,614 RGD:11554173
G Tbx22 T-box 22 JBrowse link X 78,731,738 78,782,542 RGD:724722
RGD:8554872
G Tgfb1 transforming growth factor, beta 1 JBrowse link 1 82,480,875 82,497,196 RGD:11554173
G Tgfb2 transforming growth factor, beta 2 JBrowse link 13 105,039,639 105,142,010 RGD:11554173
G Tgfb3 transforming growth factor, beta 3 JBrowse link 6 109,913,757 109,936,217 RGD:12801424
RGD:11554173
G Tmco1 transmembrane and coiled-coil domains 1 JBrowse link 13 85,465,015 85,559,113 RGD:8554872
G Tp63 tumor protein p63 JBrowse link 11 78,234,853 78,456,559 RGD:11554173
G Tyms thymidylate synthetase JBrowse link 9 121,918,875 121,931,564 RGD:11554173
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Tp63 tumor protein p63 JBrowse link 11 78,234,853 78,456,559 RGD:7240710
RGD:8554872
RGD:11568643
RGD:11554173
Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ppp3ca protein phosphatase 3 catalytic subunit alpha JBrowse link 2 241,909,332 242,186,861 RGD:8554872
RGD:7240710
Bamforth-Lazarus syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Bche butyrylcholinesterase JBrowse link 2 171,104,476 171,196,186 RGD:11554173
G Foxe1 forkhead box E1 JBrowse link 5 61,954,549 61,957,357 RGD:7240710
RGD:8554872
RGD:11554173
Basel-Vanagaite-Smirin-Yosef syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Med25 mediator complex subunit 25 JBrowse link 1 100,872,240 100,887,864 RGD:8554872
RGD:7240710
blepharocheilodontic syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cdh1 cadherin 1 JBrowse link 19 38,768,467 38,838,395 RGD:8554872
blepharocheilodontic syndrome 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cdh1 cadherin 1 JBrowse link 19 38,768,467 38,838,395 RGD:7240710
blepharocheilodontic syndrome 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ctnnd1 catenin delta 1 JBrowse link 3 72,001,904 72,053,047 RGD:8554872
RGD:7240710
Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Meis2 Meis homeobox 2 JBrowse link 3 107,560,172 107,762,732 RGD:8554872
RGD:7240710
Cleft Palate with Ankyloglossia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Tbx22 T-box 22 JBrowse link X 78,731,738 78,782,542 RGD:8554872
Cleft Palate, Psychomotor Retardation, and Distinctive Facial Features term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Kdm1a lysine demethylase 1A JBrowse link 5 154,909,003 154,965,171 RGD:7240710
RGD:8554872
cleft soft palate term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Plod2 procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 JBrowse link 8 99,977,334 100,059,736 RGD:8554872
G Tgfbr2 transforming growth factor, beta receptor 2 JBrowse link 8 124,310,288 124,399,345 RGD:13592920
Congenital Symmetric Circumferential Skin Creases 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Tubb5 tubulin, beta 5 class I JBrowse link 20 3,422,448 3,426,420 RGD:7240710
Congenital Symmetric Circumferential Skin Creases 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mapre2 microtubule-associated protein, RP/EB family, member 2 JBrowse link 18 14,814,149 15,780,290 RGD:7240710
RGD:8554872
Diamond-Blackfan Anemia with Microtia and Cleft Palate term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G LOC100361854 ribosomal protein S26-like JBrowse link X 115,495,660 115,496,062 RGD:8554872
G Rps28 ribosomal protein S28 JBrowse link 7 18,682,071 18,683,440 RGD:8554872
G Tsr2 TSR2, ribosome maturation factor JBrowse link X 20,141,406 20,146,082 RGD:8554872
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Tp63 tumor protein p63 JBrowse link 11 78,234,853 78,456,559 RGD:1600403
RGD:8554872
RGD:11532814
RGD:11568642
RGD:11568640
RGD:7240710
EEC syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Tp63 tumor protein p63 JBrowse link 11 78,234,853 78,456,559 RGD:11554173
RGD:8554872
RGD:11568639
RGD:11568638
RGD:11070288
RGD:11568075
RGD:11568074
Frontonasal Dysplasia 3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Alx1 ALX homeobox 1 JBrowse link 7 44,751,865 44,771,458 RGD:7240710
RGD:8554872
Gordon Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Piezo2 piezo-type mechanosensitive ion channel component 2 JBrowse link 18 58,353,361 58,728,555 RGD:7240710
RGD:8554872
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fgfr1 Fibroblast growth factor receptor 1 JBrowse link 16 71,265,390 71,319,046 RGD:8554872
RGD:7240710
isolated cleft palate term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Pdgfra platelet derived growth factor receptor alpha JBrowse link 14 35,527,926 35,581,130 RGD:8554872
G Satb2 SATB homeobox 2 JBrowse link 9 63,456,877 63,642,193 RGD:13592920
RGD:8554872
Kniest dysplasia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Col2a1 collagen type II alpha 1 chain JBrowse link 7 139,454,945 139,484,403 RGD:7240710
RGD:8554872
RGD:11554173
Larsen syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Chst3 carbohydrate sulfotransferase 3 JBrowse link 20 29,731,828 29,768,656 RGD:8554872
G Flnb filamin B JBrowse link 15 18,750,152 18,883,019 RGD:7240710
RGD:8554872
RGD:11554173
Microtia, Hearing Impairment, and Cleft Palate term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hoxa1 homeobox A1 JBrowse link 4 82,124,358 82,127,182 RGD:8554872
G Hoxa2 homeobox A2 JBrowse link 4 82,130,441 82,134,846 RGD:7240710
RGD:8554872
RGD:11554173
Native American myopathy term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Stac3 SH3 and cysteine rich domain 3 JBrowse link 7 70,807,427 70,815,271 RGD:7240710
RGD:8554872
Oculomaxillofacial Dysostosis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like JBrowse link 20 14,287,470 14,393,879 RGD:7240710
RGD:8554872
Opitz GBBB Syndrome, Type I term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mid1 midline 1 JBrowse link X 25,458,782 25,839,941 RGD:7240710
RGD:8554872
Periventricular Nodular Heterotopia with Syndactyly, Cleft Palate and Developmental Delay term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Nedd4l neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase JBrowse link 18 60,392,376 60,719,720 RGD:8554872
popliteal pterygium syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Irf6 interferon regulatory factor 6 JBrowse link 13 111,870,121 111,889,328 RGD:7240710
RGD:8554872
G Ripk4 receptor-interacting serine-threonine kinase 4 JBrowse link 11 38,251,991 38,274,234 RGD:8554872
RGD:13592920
Popliteal Pterygium Syndrome, Lethal Type term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ripk4 receptor-interacting serine-threonine kinase 4 JBrowse link 11 38,251,991 38,274,234 RGD:7240710
RGD:8554872
Raine Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fam20c FAM20C, golgi associated secretory pathway kinase JBrowse link 12 17,913,771 17,972,733 RGD:7240710
RGD:8554872
RGD:11560486
Rapp-Hodgkin syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Tp63 tumor protein p63 JBrowse link 11 78,234,853 78,456,559 RGD:7240710
RGD:11554173
Uveal Coloboma, with Cleft Lip and Palate and Mental Retardation term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Yap1 yes-associated protein 1 JBrowse link 8 6,133,014 6,204,240 RGD:7240710
RGD:8554872
Van der Woude syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Grhl3 grainyhead-like transcription factor 3 JBrowse link 5 153,893,039 153,925,045 RGD:13592920
RGD:8554872
G Irf6 interferon regulatory factor 6 JBrowse link 13 111,870,121 111,889,328 RGD:7240710
RGD:8554872
RGD:11554173
G LOC100125367 hypothetical protein LOC100125367 JBrowse link 13 111,890,825 111,893,308 RGD:8554872
Van der Woude Syndrome 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cfap57 cilia and flagella associated protein 57 JBrowse link 5
5
137,383,065
137,652,118
137,458,594
137,670,067
RGD:8554872
G Grhl3 grainyhead-like transcription factor 3 JBrowse link 5 153,893,039 153,925,045 RGD:7240710
RGD:8554872
X-linked cleft palate with or without ankyloglossia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Tbx22 T-box 22 JBrowse link X 78,731,738 78,782,542 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14920
    physical disorder 746
      orofacial cleft 110
        cleft palate 90
          Aase Smith Syndrome 0
          Acromegaloid Features, Overgrowth, Cleft Palate, and Hernia 0
          Ankyloblepharon Filiforme Adnatum 0
          Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development 1
          Aughton Syndrome 0
          Baetz-Greenwalt syndrome 0
          Bamforth-Lazarus syndrome 2
          Baraitser Rodeck Garner syndrome 0
          Basel-Vanagaite-Smirin-Yosef syndrome 1
          Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies 1
          Cleft Lip with or without Cleft Palate, Nonsyndromic, 7 0
          Cleft Palate with Ankyloglossia 1
          Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 0
          Cleft Palate, Deafness, and Oligodontia 0
          Cleft Palate, Midfacial Hypoplasia, Triangular Facies, and Sensorineural Hearing Loss 0
          Cleft Palate, Psychomotor Retardation, and Distinctive Facial Features 1
          Coloboma of Macula and Skeletal Anomalies 0
          Coloboma, Cleft Lip/Palate and Mental Retardation Syndrome 0
          Congenital Hydronephrosis, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation 0
          Congenital Symmetric Circumferential Skin Creases + 2
          Craniosynostosis Mental Retardation Clefting Syndrome 0
          Crumpled Helices and Small Mouth 0
          Diamond-Blackfan Anemia with Microtia and Cleft Palate 3
          Dyssegmental Dysplasia, Rolland-Desbuquois Type 0
          EEC syndrome + 1
          Ectrodactyly-Cleft Palate Syndrome 0
          Emanuel Syndrome 0
          Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly 0
          Faciocardiorenal Syndrome 0
          Familial Lissencephaly with Cleft Palate and Cerebellar Hypoplasia 0
          Familial Popliteal Pterygium Syndrome 0
          Feingold Trainer Syndrome 0
          Frontonasal Dysplasia 3 1
          Genito Palato Cardiac Syndrome 0
          Gordon Syndrome 1
          Halal Syndrome 0
          Hardikar Syndrome 0
          Hay Wells Syndrome Recessive Type 0
          Ho Kaufman Mcalister Syndrome 0
          Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate 1
          Holzgreve-Wagner-Rehder syndrome 0
          Hypodontia Oligodontia with Orofacial Cleft 0
          Hypotrichosis, Progressive Patterned Scalp, with Wiry Hair, Onycholysis, and Cleft Lip/Palate 0
          Iida Kannari Syndrome 0
          Kallmann Syndrome 2 with Cleft Lip or Palate 0
          Kapur Toriello Syndrome 0
          Kniest dysplasia 1
          Kuster Syndrome 0
          Ladda Zonana Ramer syndrome 0
          Larsen syndrome 2
          Lowry Maclean syndrome 0
          Macrosomia with Lethal Microphthalmia 0
          Martinez Monasterio Pinheiro Syndrome 0
          McPherson Clemens Syndrome 0
          Microcephaly, Corpus Callosum Dysgenesis and Cleft Lip-Palate 0
          Microtia, Hearing Impairment, and Cleft Palate 2
          Multiple Epiphyseal Dysplasia with Robin Phenotype 0
          Native American myopathy 1
          Oculomaxillofacial Dysostosis 1
          Oculopalatocerebral Syndrome 0
          Omphalocele, Cleft Palate Syndrome Lethal 0
          Opitz GBBB Syndrome, Type I 1
          PARC Syndrome 0
          Palant Cleft Palate Syndrome 0
          Periventricular Nodular Heterotopia with Syndactyly, Cleft Palate and Developmental Delay 1
          Piepkorn Karp Hickok syndrome 0
          Pilotto Syndrome 0
          Raine Syndrome 1
          Rapp-Hodgkin syndrome 1
          Reardon Hall Slaney syndrome 0
          Rosselli-Gulienetti Syndrome 0
          Sakoda Complex 0
          Samson Viljoen Syndrome 0
          Say Syndrome 0
          Schilbach-Rott Syndrome Ocular Hypotelorism, Submucosal Cleft Palate, and Hypospadias 0
          Schrander-Stumpel Theunissen Hulsmans Syndrome 0
          Selective Tooth Agenesis with Orofacial Cleft 0
          Seres-Santamaria Arimany Muniz Syndrome 0
          Spondyloepiphyseal Dysplasia with Coronal Craniosynostosis, Cataracts, Cleft Palate, and Mental Retardation 0
          Uveal Coloboma, with Cleft Lip and Palate and Mental Retardation 1
          Van der Woude Syndrome 2 2
          Van der Woude syndrome + 4
          X-linked cleft palate with or without ankyloglossia 1
          Yim Ebbin Syndrome 0
          Zadik Barak Levin Syndrome 0
          ankyloblepharon-ectodermal defects-cleft lip/palate syndrome 1
          blepharocheilodontic syndrome + 2
          cleft soft palate 2
          ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 0
          ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 1
          hypertelorism, microtia, facial clefting syndrome 0
          isolated cleft palate 2
          popliteal pterygium syndrome + 2
Path 2
Term Annotations click to browse term
  disease 14920
    Developmental Diseases 7769
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7091
        Congenital Abnormalities 3197
          Musculoskeletal Abnormalities 1196
            Craniofacial Abnormalities 953
              Maxillofacial Abnormalities 202
                Jaw Abnormalities 199
                  orofacial cleft 110
                    cleft palate 90
                      Aase Smith Syndrome 0
                      Acromegaloid Features, Overgrowth, Cleft Palate, and Hernia 0
                      Ankyloblepharon Filiforme Adnatum 0
                      Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development 1
                      Aughton Syndrome 0
                      Baetz-Greenwalt syndrome 0
                      Bamforth-Lazarus syndrome 2
                      Baraitser Rodeck Garner syndrome 0
                      Basel-Vanagaite-Smirin-Yosef syndrome 1
                      Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies 1
                      Cleft Lip with or without Cleft Palate, Nonsyndromic, 7 0
                      Cleft Palate with Ankyloglossia 1
                      Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 0
                      Cleft Palate, Deafness, and Oligodontia 0
                      Cleft Palate, Midfacial Hypoplasia, Triangular Facies, and Sensorineural Hearing Loss 0
                      Cleft Palate, Psychomotor Retardation, and Distinctive Facial Features 1
                      Coloboma of Macula and Skeletal Anomalies 0
                      Coloboma, Cleft Lip/Palate and Mental Retardation Syndrome 0
                      Congenital Hydronephrosis, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation 0
                      Congenital Symmetric Circumferential Skin Creases + 2
                      Craniosynostosis Mental Retardation Clefting Syndrome 0
                      Crumpled Helices and Small Mouth 0
                      Diamond-Blackfan Anemia with Microtia and Cleft Palate 3
                      Dyssegmental Dysplasia, Rolland-Desbuquois Type 0
                      EEC syndrome + 1
                      Ectrodactyly-Cleft Palate Syndrome 0
                      Emanuel Syndrome 0
                      Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly 0
                      Faciocardiorenal Syndrome 0
                      Familial Lissencephaly with Cleft Palate and Cerebellar Hypoplasia 0
                      Familial Popliteal Pterygium Syndrome 0
                      Feingold Trainer Syndrome 0
                      Frontonasal Dysplasia 3 1
                      Genito Palato Cardiac Syndrome 0
                      Gordon Syndrome 1
                      Halal Syndrome 0
                      Hardikar Syndrome 0
                      Hay Wells Syndrome Recessive Type 0
                      Ho Kaufman Mcalister Syndrome 0
                      Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate 1
                      Holzgreve-Wagner-Rehder syndrome 0
                      Hypodontia Oligodontia with Orofacial Cleft 0
                      Hypotrichosis, Progressive Patterned Scalp, with Wiry Hair, Onycholysis, and Cleft Lip/Palate 0
                      Iida Kannari Syndrome 0
                      Kallmann Syndrome 2 with Cleft Lip or Palate 0
                      Kapur Toriello Syndrome 0
                      Kniest dysplasia 1
                      Kuster Syndrome 0
                      Ladda Zonana Ramer syndrome 0
                      Larsen syndrome 2
                      Lowry Maclean syndrome 0
                      Macrosomia with Lethal Microphthalmia 0
                      Martinez Monasterio Pinheiro Syndrome 0
                      McPherson Clemens Syndrome 0
                      Microcephaly, Corpus Callosum Dysgenesis and Cleft Lip-Palate 0
                      Microtia, Hearing Impairment, and Cleft Palate 2
                      Multiple Epiphyseal Dysplasia with Robin Phenotype 0
                      Native American myopathy 1
                      Oculomaxillofacial Dysostosis 1
                      Oculopalatocerebral Syndrome 0
                      Omphalocele, Cleft Palate Syndrome Lethal 0
                      Opitz GBBB Syndrome, Type I 1
                      PARC Syndrome 0
                      Palant Cleft Palate Syndrome 0
                      Periventricular Nodular Heterotopia with Syndactyly, Cleft Palate and Developmental Delay 1
                      Piepkorn Karp Hickok syndrome 0
                      Pilotto Syndrome 0
                      Raine Syndrome 1
                      Rapp-Hodgkin syndrome 1
                      Reardon Hall Slaney syndrome 0
                      Rosselli-Gulienetti Syndrome 0
                      Sakoda Complex 0
                      Samson Viljoen Syndrome 0
                      Say Syndrome 0
                      Schilbach-Rott Syndrome Ocular Hypotelorism, Submucosal Cleft Palate, and Hypospadias 0
                      Schrander-Stumpel Theunissen Hulsmans Syndrome 0
                      Selective Tooth Agenesis with Orofacial Cleft 0
                      Seres-Santamaria Arimany Muniz Syndrome 0
                      Spondyloepiphyseal Dysplasia with Coronal Craniosynostosis, Cataracts, Cleft Palate, and Mental Retardation 0
                      Uveal Coloboma, with Cleft Lip and Palate and Mental Retardation 1
                      Van der Woude Syndrome 2 2
                      Van der Woude syndrome + 4
                      X-linked cleft palate with or without ankyloglossia 1
                      Yim Ebbin Syndrome 0
                      Zadik Barak Levin Syndrome 0
                      ankyloblepharon-ectodermal defects-cleft lip/palate syndrome 1
                      blepharocheilodontic syndrome + 2
                      cleft soft palate 2
                      ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 0
                      ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 1
                      hypertelorism, microtia, facial clefting syndrome 0
                      isolated cleft palate 2
                      popliteal pterygium syndrome + 2
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.