Abnormality of the palate

Symptom Information:

Symptom ID: HPO:0000174
Palate abnormality [HPO:0000174]
Palate anomaly [Orphanet:11000]
Palate anomalies [Orphanet:11000]
Palate anomalies [OMIM:Palate anomalies]
Cross references:
Orphanet:11000 "Palate anomalies" [Orphanet:11000]
OMIM: "Palate anomalies" [OMIM:Palate anomalies]
Is a (Direct Parents):
HPO         Abnormality of the oral cavity
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the mouth(HPO:0000153)
                   Abnormality of the oral cavity(HPO:0000163)
                      Abnormality of the palate(HPO:0000174)
Database Frequency: 298 / 7739

All diseases associated with this symptom:

15q14 microdeletion syndrome (Orphanet:261190)
16p13.11 microdeletion syndrome (Orphanet:261236)
17q12 microduplication syndrome (Orphanet:261272)
19p13.12 microdeletion syndrome (Orphanet:254346)
22q11.2 microduplication syndrome (Orphanet:1727)
2q31.1 microdeletion syndrome (Orphanet:251014)
2q32q33 microdeletion syndrome (Orphanet:251019)
3C syndrome (Orphanet:7)
3q29 microduplication (Orphanet:251038)
48,XXXY syndrome (Orphanet:96263)
49,XXXXY syndrome (Orphanet:96264)
6p22 microdeletion syndrome (Orphanet:251046)
6q25 microdeletion syndrome (Orphanet:251056)
8q22.1 microdeletion syndrome (Orphanet:178303)
AL amyloidosis (Orphanet:85443)
Aarskog-Scott syndrome (Orphanet:915)
Aase-Smith syndrome (Orphanet:916)
Abruzzo-Erickson syndrome (Orphanet:921)
Acalvaria (Orphanet:945)
Acro-cardio-facial syndrome (Orphanet:2008)
Acro-fronto-facio-nasal dysostosis (Orphanet:1784)
Acrocraniofacial dysostosis (Orphanet:949)
Acroosteolysis, dominant type (Orphanet:955)
Acropectorovertebral dysplasia (Orphanet:957)
Acrorenal syndrome (Orphanet:971)
Adducted thumbs - arthrogryposis, Christian type (Orphanet:2952)
Agenesis of the corpus callosum - intellectual deficit - coloboma - micrognathia (Orphanet:52055)
Aminopterin/methotrexate embryofetopathy (Orphanet:1908)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Ankyloblepharon filiforme - imperforate anus (Orphanet:1074)
Ankyloblepharon filiforme adnatum - cleft palate (Orphanet:1072)
Anophthalmia plus syndrome (Orphanet:1104)
Antley-Bixler syndrome (Orphanet:83)
Apert syndrome (Orphanet:87)
Arachnodactyly - abnormal ossification - intellectual deficit (Orphanet:1129)
Arrhinia - choanal atresia - microphthalmia (Orphanet:1135)
Arthrogryposis multiplex congenita - whistling face (Orphanet:1150)
Autosomal dominant Larsen syndrome (Orphanet:503)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal dominant popliteal pterygium syndrome (Orphanet:1300)
Autosomal dominant spondylocostal dysostosis (Orphanet:1797)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Autosomal recessive spondylocostal dysostosis (Orphanet:2311)
BOR syndrome (Orphanet:107)
BRESEK syndrome (Orphanet:85284)
Baller-Gerold syndrome (Orphanet:1225)
Beckwith-Wiedemann syndrome (Orphanet:116)
Bencze syndrome (Orphanet:1241)
Bilateral renal agenesis (Orphanet:1848)
Blackfan-Diamond anemia (Orphanet:124)
Blepharonasofacial malformation syndrome (Orphanet:1252)
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency (Orphanet:329255)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
Blepharophimosis-intellectual deficit syndrome, SBBYS type (Orphanet:3047)
Bohring-Opitz syndrome (Orphanet:97297)
Branchio-otic syndrome (Orphanet:52429)
Branchiogenic deafness syndrome (Orphanet:50815)
Brittle cornea syndrome (Orphanet:90354)
C syndrome (Orphanet:1308)
CHILD syndrome (Orphanet:139)
Campomelia, Cumming type (Orphanet:1318)
Campomelic dysplasia (Orphanet:140)
Cantrell pentalogy (Orphanet:1335)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carey-Fineman-Ziter syndrome (Orphanet:1358)
Catel-Manzke syndrome (Orphanet:1388)
Cerebro-costo-mandibular syndrome (Orphanet:1393)
Cholestasis - pigmentary retinopathy - cleft palate (Orphanet:1415)
Cleft palate - large ears - small head (Orphanet:2013)
Cleft palate - short stature - vertebral anomalies (Orphanet:2015)
Cleft palate - stapes fixation - oligodontia (Orphanet:2010)
Cleft palate-lateral synechia syndrome (Orphanet:2016)
Cleidocranial dysplasia (Orphanet:1452)
Coffin-Siris syndrome (Orphanet:1465)
Congenital laryngomalacia (Orphanet:2373)
Congenital unilateral hypoplasia of depressor anguli oris (Orphanet:1166)
Congenital velopharyngeal incompetence (Orphanet:2291)
Contractures - ectodermal dysplasia - cleft lip/palate (Orphanet:1484)
Cornelia de Lange syndrome (Orphanet:199)
Crane-Heise syndrome (Orphanet:1512)
Craniomicromelic syndrome (Orphanet:1524)
Craniosynostosis - anal anomalies - porokeratosis (Orphanet:85199)
Craniosynostosis - fibular aplasia (Orphanet:1533)
Craniosynostosis, Boston type (Orphanet:1541)
Craniosynostosis, Herrmann-Opitz type (Orphanet:2145)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
Deafness - onychodystrophy (Orphanet:3231)
Desmosterolosis (Orphanet:35107)
Diabetic embryopathy (Orphanet:1926)
Diaphanospondylodysostosis (Orphanet:66637)
Diastrophic dwarfism (Orphanet:628)
Diprosopia (Orphanet:1681)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal limb deficiencies - micrognathia syndrome (Orphanet:1307)
Distal monosomy 10p (Orphanet:1580)
Distal monosomy 19p13.3 (Orphanet:96129)
Distal monosomy 3p (Orphanet:1620)
Distal monosomy 9p (Orphanet:1642)
Duane retraction syndrome (Orphanet:233)
Dubowitz syndrome (Orphanet:235)
Dysmorphism - cleft palate - loose skin (Orphanet:1779)
Dysmorphism - short stature - deafness - disorder of sex development (Orphanet:2282)
Dysostosis, Stanescu type (Orphanet:1798)
Dyssegmental dysplasia, Silverman-Handmaker type (Orphanet:1865)
EEC syndrome (Orphanet:1896)
Ear-patella-short stature syndrome (Orphanet:2554)
Ectodermal dysplasia - intellectual deficit - central nervous system malformation (Orphanet:1812)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Eye defects - arachnodactyly - cardiopathy (Orphanet:2725)
Faciocardiorenal syndrome (Orphanet:1973)
Familial visceral myopathy (Orphanet:2604)
Fanconi anemia (Orphanet:84)
Femoral-facial syndrome (Orphanet:1988)
Fetal akinesia deformation sequence (Orphanet:994)
Fetal alcohol syndrome (Orphanet:1915)
Fetal hydantoin syndrome (Orphanet:1912)
Fibrochondrogenesis (Orphanet:2021)
Fine-Lubinsky syndrome (Orphanet:1272)
Fronto-facio-nasal dysostosis (Orphanet:1791)
Frontonasal dysplasia (Orphanet:250)
Fryns syndrome (Orphanet:2059)
Gamma heavy-chain disease (Orphanet:100026)
Genito-palato-cardiac syndrome (Orphanet:2075)
Goldberg-Shprintzen megacolon syndrome (Orphanet:66629)
Goldenhar syndrome (Orphanet:374)
Gonadal dysgenesis, XY type - associated anomalies (Orphanet:1770)
Gordon syndrome (Orphanet:376)
Grix-Blankenship-Peterson syndrome (Orphanet:2099)
Hamel cerebro-palato-cardiac syndrome (Orphanet:93946)
Hartsfield-Bixler-Demyer syndrome (Orphanet:2117)
Hemimelia (Orphanet:2130)
Holoprosencephaly - caudal dysgenesis (Orphanet:2165)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Holzgreve-Wagner-Rehder syndrome (Orphanet:2167)
Humerus trochlea aplasia (Orphanet:3383)
Hydrolethalus (Orphanet:2189)
Hypoglossia - hypodactyly (Orphanet:989)
Hypomandibular faciocranial dysostosis (Orphanet:1790)
Hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism (Orphanet:2250)
Intellectual deficit - cataracts - calcified pinnae - myopathy (Orphanet:3042)
Intellectual deficit, X-linked - hypogammaglobulinemia - progressive neurological deterioration (Orphanet:85317)
Intellectual deficit, X-linked, Abidi type (Orphanet:85273)
Intellectual deficit, X-linked, Armfield type (Orphanet:85276)
Intellectual deficit, X-linked, Siderius type (Orphanet:85287)
Isolated Dandy-Walker malformation (Orphanet:217)
Isolated Klippel-Feil syndrome (Orphanet:2345)
Isolated Pierre Robin syndrome (Orphanet:718)
Isotretinoin syndrome (Orphanet:2305)
Joubert syndrome with orofaciodigital defect (Orphanet:2754)
Juberg-Hayward syndrome (Orphanet:2319)
KBG syndrome (Orphanet:2332)
Kabuki syndrome (Orphanet:2322)
Kallmann syndrome (Orphanet:478)
Keratoderma hereditarium mutilans (Orphanet:494)
Kniest dysplasia (Orphanet:485)
Koolen-De Vries syndrome (Orphanet:96169)
Lateral meningocele syndrome (Orphanet:2789)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Leprechaunism (Orphanet:508)
Lethal Kniest-like dysplasia (Orphanet:2347)
Lethal Larsen-like syndrome (Orphanet:2371)
Lethal chondrodysplasia, Moerman type (Orphanet:1420)
Lethal multiple pterygium syndrome (Orphanet:33108)
Lethal omphalocele-cleft palate syndrome (Orphanet:2736)
Lethal restrictive dermopathy (Orphanet:1662)
Limb body wall complex (Orphanet:2369)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
Lowry-MacLean syndrome (Orphanet:2409)
Macrosomia - microphthalmia - cleft palate (Orphanet:2432)
Mal de Meleda (Orphanet:87503)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
Mandibulofacial dysostosis-microcephaly syndrome (Orphanet:79113)
Marden-Walker syndrome (Orphanet:2461)
Marfan syndrome (Orphanet:558)
Marshall syndrome (Orphanet:560)
Maternal hyperthermia induced birth defects (Orphanet:2216)
Maxillo-nasal dysplasia (Orphanet:1248)
McCune-Albright syndrome (Orphanet:562)
McKusick-Kaufman syndrome (Orphanet:2473)
Meckel syndrome (Orphanet:564)
Medeira-Dennis-Donnai syndrome (Orphanet:2476)
Menkes disease (Orphanet:565)
Mesomelic dwarfism - cleft palate - camptodactyly (Orphanet:2631)
Metatropic dysplasia (Orphanet:2635)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Microcephaly - cardiac defect - lung malsegmentation (Orphanet:2516)
Microcephaly - cleft palate (Orphanet:2521)
Microphthalmia with limb anomalies (Orphanet:1106)
Mitochondrial myopathy and sideroblastic anemia (Orphanet:2598)
Moebius syndrome (Orphanet:570)
Monosomy 18p (Orphanet:1598)
Monosomy 9p (Orphanet:261112)
Mosaic trisomy 14 (Orphanet:1703)
Mosaic trisomy 8 (Orphanet:96061)
Mosaic trisomy 9 (Orphanet:99776)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Mucolipidosis type 3 (Orphanet:577)
Multiple benign circumferential skin creases on limbs (Orphanet:2505)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Multiple epiphyseal dysplasia type 4 (Orphanet:93307)
Multiple epiphyseal dysplasia, Lowry type (Orphanet:166016)
Myhre syndrome (Orphanet:2588)
Nager syndrome (Orphanet:245)
Nephrosis - deafness - urinary tract - digital malformations (Orphanet:2669)
Neu-Laxova syndrome (Orphanet:2671)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Nijmegen breakage syndrome (Orphanet:647)
Oculo-palato-cerebral syndrome (Orphanet:2714)
Oculoauriculovertebral spectrum with radial defects (Orphanet:2549)
Oculodentodigital dysplasia (Orphanet:2710)
Oculofaciocardiodental syndrome (Orphanet:2712)
Oculomaxillofacial dysostosis (Orphanet:1794)
Okamoto syndrome (Orphanet:2729)
Opitz G/BBB syndrome (Orphanet:2745)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 10 (Orphanet:2756)
Orofaciodigital syndrome type 2 (Orphanet:2751)
Orofaciodigital syndrome type 3 (Orphanet:2752)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Osteocraniostenosis (Orphanet:2763)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 1 (Orphanet:90650)
Otopalatodigital syndrome type 2 (Orphanet:90652)
Otospondylomegaepiphyseal dysplasia (Orphanet:1427)
PARC syndrome (Orphanet:2825)
Pai syndrome (Orphanet:1993)
Pallister-Hall syndrome (Orphanet:672)
Patterson-Stevenson-Fontaine syndrome (Orphanet:2439)
Pelvis-shoulder dysplasia (Orphanet:2839)
Pfeiffer syndrome type 2 (Orphanet:93259)
Pfeiffer syndrome type 3 (Orphanet:93260)
Phocomelia, Schinzel type (Orphanet:2879)
Pilotto syndrome (Orphanet:2894)
Pitt-Hopkins syndrome (Orphanet:2896)
Platyspondylic dysplasia, Torrance type (Orphanet:85166)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
Primary localized amyloidosis (Orphanet:314709)
Proximal 16p11.2 microdeletion syndrome (Orphanet:261197)
RAPADILINO syndrome (Orphanet:3021)
Recombinant 8 syndrome (Orphanet:96167)
Renpenning syndrome (Orphanet:3242)
Rhizomelic syndrome, Urbach type (Orphanet:3098)
Richieri Costa-Pereira syndrome (Orphanet:3102)
Robin sequence - oligodactyly (Orphanet:3104)
Saethre-Chotzen syndrome (Orphanet:794)
Schilbach-Rott syndrome (Orphanet:2353)
Schisis association (Orphanet:63862)
Schneckenbecken dysplasia (Orphanet:3144)
Schwartz-Jampel syndrome (Orphanet:800)
Septo-optic dysplasia (Orphanet:3157)
Severe intellectual deficit - epilepsy - anal anomalies - distal phalangeal hypoplasia (Orphanet:94066)
Short rib-polydactyly syndrome (Orphanet:1505)
Short stature - craniofacial anomalies - genital hypoplasia (Orphanet:2994)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Solitary median maxillary central incisor syndrome (Orphanet:2286)
Spondylocarpotarsal synostosis (Orphanet:3275)
Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Orphanet:93346)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia (Orphanet:253)
Spondyloepiphyseal dysplasia congenita (Orphanet:94068)
Sprengel deformity (Orphanet:3181)
Stickler syndrome (Orphanet:828)
Stickler syndrome type 1 (Orphanet:90653)
Stickler syndrome type 2 (Orphanet:90654)
Stickler syndrome type 3 (Orphanet:166100)
TARP syndrome (Orphanet:2886)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Tetraploidy (Orphanet:3305)
Thrombocytopenia - Robin sequence (Orphanet:3323)
Thrombocytopenia - absent radius (Orphanet:3320)
Toriello-Carey syndrome (Orphanet:3338)
Treacher-Collins syndrome (Orphanet:861)
Triopia (Orphanet:3374)
Triploidy (Orphanet:3376)
Trisomy 12p (Orphanet:1699)
Trisomy 13 (Orphanet:3378)
Trisomy 17p (Orphanet:261290)
Trisomy 18 (Orphanet:3380)
Trisomy 1q (Orphanet:261344)
Trisomy 8q (Orphanet:1752)
Tumoral calcinosis (Orphanet:53715)
VACTERL/VATER association (Orphanet:887)
Van den Ende-Gupta syndrome (Orphanet:2460)
Van der Woude syndrome (Orphanet:888)
Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence (Orphanet:3201)
Verloove Vanhorick-Brubakk syndrome (Orphanet:3429)
W syndrome (Orphanet:2804)
Waardenburg syndrome type 1 (Orphanet:894)
Walker-Warburg syndrome (Orphanet:899)
Weaver-Williams syndrome (Orphanet:3448)
Wolf-Hirschhorn syndrome (Orphanet:280)
Zlotogora-Ogur syndrome (Orphanet:3253)
Zunich-Kaye syndrome (Orphanet:3474)