Abnormality of the palate
Symptom Information:
Symptom ID: | HPO:0000174 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) 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) MedDRA: |
||||
Database Frequency: | 298 / 7739 | ||||
Resource: |
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) |