High, narrow palate

Symptom Information:

Symptom ID: HPO:0002705
High palate [Orphanet:11150]
Narrow palate [Orphanet:11150]
Byzanthine arch palate (disorder) [Orphanet:11150]
Byzanthine arch palate [Orphanet:11150]
High, narrow palate [OMIM:High, narrow palate]
High vaulted/narrow palate [Orphanet:11150]
High arched palate [Orphanet:11150]
High arched palate [MedDRA:10020046]
High arched palate (in some patients) [OMIM:High arched palate (in some patients)]
High palate (in some patients) [OMIM:High palate (in some patients)]
High, narrow palate (50%) [OMIM:High, narrow palate (50%)]
High-arched palate (1 family) [OMIM:High-arched palate (1 family)]
High-arched palate (1 patient) [OMIM:High-arched palate (1 patient)]
High-arched palate (12% of patients) [OMIM:High-arched palate (12% of patients)]
High-arched palate (15%) [OMIM:High-arched palate (15%)]
High-arched palate (17%) [OMIM:High-arched palate (17%)]
High-arched palate (28%) [OMIM:High-arched palate (28%)]
High-arched palate (3 patients) [OMIM:High-arched palate (3 patients)]
High-arched palate (52%) [OMIM:High-arched palate (52%)]
High-arched palate (61%) [OMIM:High-arched palate (61%)]
High-arched palate (in some patients) [OMIM:High-arched palate (in some patients)]
High-arched palate (rare) [OMIM:High-arched palate (rare)]
Narrow palate (46%) [OMIM:Narrow palate (46%)]
Cross references:
HPO:0000156 "High-arched palate" [Orphanet:11150]
HPO:0000218 "High palate" [Orphanet:11150]
HPO:0000189 "Narrow palate" [Orphanet:11150]
HPO:0009080 "Narrow, high-arched palate" [Orphanet:11150]
Orphanet:11150 "High vaulted/narrow palate" [Orphanet:11150]
OMIM: "High, narrow palate" [OMIM:High, narrow palate]
OMIM: "High arched palate (in some patients)" [OMIM:High arched palate (in some patients)]
OMIM: "High palate (in some patients)" [OMIM:High palate (in some patients)]
OMIM: "High, narrow palate (50%)" [OMIM:High, narrow palate (50%)]
OMIM: "High-arched palate (1 family)" [OMIM:High-arched palate (1 family)]
OMIM: "High-arched palate (1 patient)" [OMIM:High-arched palate (1 patient)]
OMIM: "High-arched palate (12% of patients)" [OMIM:High-arched palate (12% of patients)]
OMIM: "High-arched palate (15%)" [OMIM:High-arched palate (15%)]
OMIM: "High-arched palate (17%)" [OMIM:High-arched palate (17%)]
OMIM: "High-arched palate (28%)" [OMIM:High-arched palate (28%)]
OMIM: "High-arched palate (3 patients)" [OMIM:High-arched palate (3 patients)]
OMIM: "High-arched palate (52%)" [OMIM:High-arched palate (52%)]
OMIM: "High-arched palate (61%)" [OMIM:High-arched palate (61%)]
OMIM: "High-arched palate (in some patients)" [OMIM:High-arched palate (in some patients)]
OMIM: "High-arched palate (rare)" [OMIM:High-arched palate (rare)]
OMIM: "Narrow palate (46%)" [OMIM:Narrow palate (46%)]
UMLS:C0240635 "Byzanthine arch palate" [Orphanet:11150]
Is a (Direct Parents):
MedDRA Palate disorders congenital
Orphanet Narrow palate
Orphanet Abnormality of the palate
HPO         High palate
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)
                         High palate(HPO:0000218)
                            High, narrow palate(HPO:0002705)
Congenital, familial and genetic disorders(MedDRA:10010331)
    Gastrointestinal tract disorders congenital(MedDRA:10018018)
       Palate disorders congenital(MedDRA:10033530)
          High, narrow palate(HPO:0002705)
Database Frequency: 308 / 7739

All diseases associated with this symptom:

14q11.2 microdeletion syndrome (Orphanet:261120)
15q24 microdeletion syndrome (Orphanet:94065)
16q24.3 microdeletion syndrome (Orphanet:261250)
17p13.3 microduplication syndrome (Orphanet:217385)
17q12 microdeletion syndrome (Orphanet:261265)
17q21.31 microduplication syndrome (Orphanet:217340)
1q21.1 microdeletion syndrome (Orphanet:250989)
1q44 microdeletion syndrome (Orphanet:238769)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2q32q33 microdeletion syndrome (Orphanet:251019)
2q37 microdeletion syndrome (Orphanet:1001)
3C syndrome (Orphanet:7)
3q29 microdeletion syndrome (Orphanet:65286)
3q29 microduplication (Orphanet:251038)
5p13 microduplication syndrome (Orphanet:329802)
6q16 deletion syndrome (Orphanet:171829)
6q25 microdeletion syndrome (Orphanet:251056)
8p11.2 deletion syndrome (Orphanet:251066)
8p23.1 microdeletion syndrome (Orphanet:251071)
8q21.11 microdeletion syndrome (Orphanet:284160)
Abruzzo-Erickson syndrome (Orphanet:921)
Acro-fronto-facio-nasal dysostosis (Orphanet:1784)
Acro-oto-ocular syndrome (Orphanet:2980)
Acro-renal-mandibular syndrome (Orphanet:958)
Acrofacial dysostosis, Catania type (Orphanet:1786)
Acrofacial dysostosis, Palagonia type (Orphanet:1787)
Acropectorovertebral dysplasia (Orphanet:957)
Adducted thumbs - arthrogryposis, Christian type (Orphanet:2952)
Agenesis of the corpus callosum - intellectual deficit - coloboma - micrognathia (Orphanet:52055)
Alexander disease (Orphanet:58)
Alpha-mannosidosis (Orphanet:61)
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 (Orphanet:98791)
Anophthalmia - megalocornea - cardiopathy - skeletal anomalies (Orphanet:1101)
Apert syndrome (Orphanet:87)
Arrhinia - choanal atresia - microphthalmia (Orphanet:1135)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Ascher syndrome (Orphanet:1253)
Ataxia - photosensitivity - short stature (Orphanet:1184)
Ataxia-deafness-retardation syndrome (Orphanet:1188)
Autosomal agammaglobulinemia (Orphanet:33110)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive centronuclear myopathy (Orphanet:169186)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
Baller-Gerold syndrome (Orphanet:1225)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Barber-Say syndrome (Orphanet:1231)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 4 (OMIM:615982)
Bardet-Biedl syndrome 7 (OMIM:615984)
Bird headed-dwarfism, Montreal type (Orphanet:2617)
Brachydactyly - mesomelia - intellectual deficit - heart defects (Orphanet:1277)
Brachydactyly - preaxial hallux varus (Orphanet:1278)
Branchio-oculo-facial syndrome (Orphanet:1297)
Böök syndrome (Orphanet:1262)
C syndrome (Orphanet:1308)
Camptodactyly - joint contractures - facial skeletal defects (Orphanet:1323)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Cardiospondylocarpofacial syndrome (Orphanet:3238)
Carey-Fineman-Ziter syndrome (Orphanet:1358)
Cartilage-hair hypoplasia (Orphanet:175)
Cataract - hypertrichosis - intellectual deficit (Orphanet:1375)
Cataract - intellectual deficit - anal atresia - urinary defects (Orphanet:1381)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Cenani-Lenz syndrome (Orphanet:3258)
Cerebro-oculo-nasal syndrome (Orphanet:66625)
Cerebro-reno-digital syndrome (Orphanet:1396)
Choanal atresia - deafness - cardiac defects - dysmorphism (Orphanet:1200)
Classical homocystinuria (Orphanet:394)
Cleidocranial dysplasia (Orphanet:1452)
Cockayne syndrome (Orphanet:191)
Coffin-Lowry syndrome (Orphanet:192)
Cohen syndrome (Orphanet:193)
Conductive deafness - malformed external ear (Orphanet:3216)
Conductive deafness - ptosis - skeletal anomalies (Orphanet:3236)
Congenital contractural arachnodactyly (Orphanet:115)
Congenital multicore myopathy with external ophthalmoplegia (Orphanet:98905)
Cornelia de Lange syndrome (Orphanet:199)
Corpus callosum agenesis - double urinary collecting system (Orphanet:1492)
Cortical blindness - intellectual deficit - polydactyly (Orphanet:1389)
Costello syndrome (Orphanet:3071)
Cowden syndrome (Orphanet:201)
Craniofrontonasal dysplasia (Orphanet:1520)
Craniolenticulosutural dysplasia (Orphanet:50814)
Craniosynostosis - fibular aplasia (Orphanet:1533)
Crouzon disease (Orphanet:207)
Crouzon syndrome - acanthosis nigricans (Orphanet:93262)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Cutis laxa (Orphanet:209)
DPM1-CDG (Orphanet:79322)
Deaf blind hypopigmentation syndrome, Yemenite type (Orphanet:3214)
Deafness - onychodystrophy (Orphanet:3231)
Deafness-craniofacial syndrome (Orphanet:3241)
Delayed speech - facial asymmetry - strabismus - ear lobe creases (Orphanet:3038)
Dislocation of the hip - dysmorphism (Orphanet:2412)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal 22q11.2 microduplication syndrome (Orphanet:261337)
Distal limb deficiencies - micrognathia syndrome (Orphanet:1307)
Distal monosomy 3p (Orphanet:1620)
Distal monosomy 9p (Orphanet:1642)
Distal trisomy 15q (Orphanet:1707)
Distal trisomy 18q (Orphanet:1716)
Down syndrome (Orphanet:870)
Dubowitz syndrome (Orphanet:235)
Ear-patella-short stature syndrome (Orphanet:2554)
Ectrodactyly - spina bifida - cardiopathy (Orphanet:1894)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Emery-Nelson syndrome (Orphanet:1927)
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria (Orphanet:1035)
Endomyocardial fibroelastosis (Orphanet:2022)
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation (Orphanet:1970)
Fallot complex - intellectual deficit - growth delay (Orphanet:3304)
Familial scaphocephaly syndrome, McGillivray type (Orphanet:168624)
Fanconi anemia (Orphanet:84)
Fetal Gaucher disease (Orphanet:85212)
Fetal trimethadione syndrome (Orphanet:1913)
Flat face - microstomia - ear anomaly (Orphanet:1968)
Fountain syndrome (Orphanet:3219)
Fraser syndrome (Orphanet:2052)
Fried syndrome (Orphanet:85335)
Frontometaphyseal dysplasia (Orphanet:1826)
Fryns syndrome (Orphanet:2059)
Fukuda-Miyanomae-Nakata syndrome (Orphanet:2060)
GAPO syndrome (Orphanet:2067)
German syndrome (Orphanet:2077)
Gingival fibromatosis - facial dysmorphism (Orphanet:2025)
Glaucoma secondary to spherophakia/ectopia lentis and megalocornea (Orphanet:238763)
Gordon syndrome (Orphanet:376)
Grant syndrome (Orphanet:2097)
Hallermann-Streiff syndrome (Orphanet:2108)
Harrod syndrome (Orphanet:2115)
Heart-hand syndrome type 2 (Orphanet:1350)
Hennekam-Beemer syndrome (Orphanet:2135)
Hereditary sensory and autonomic neuropathy type 6 (Orphanet:314381)
Hirschsprung disease - nail hypoplasia - dysmorphism (Orphanet:2153)
Hirsutism - skeletal dysplasia - intellectual deficit (Orphanet:2156)
Hurler syndrome (Orphanet:93473)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Hydrocephaly - tall stature - joint laxity (Orphanet:2181)
Hypoglossia - hypodactyly (Orphanet:989)
Hypogonadism - mitral valve prolapse - intellectual deficit (Orphanet:2233)
Hypospadias - intellectual deficit, Goldblatt type (Orphanet:2261)
Hypotonia-cerebral atrophy-hyperglycinemia syndrome (Orphanet:363424)
Ichthyosis-cheek-eyebrow syndrome (Orphanet:2267)
Intellectual deficit - athetosis - microphthalmia (Orphanet:1236)
Intellectual deficit - balding - patella luxation - acromicria (Orphanet:3041)
Intellectual deficit - hypoplastic corpus callosum - preauricular tag (Orphanet:1495)
Intellectual deficit - hypotonia - skin hyperpigmentation (Orphanet:3050)
Intellectual deficit - myopathy - short stature - endocrine defect (Orphanet:3068)
Intellectual deficit - polydactyly - uncombable hair (Orphanet:3082)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Intellectual deficit, X-linked - cubitus valgus - dysmorphism (Orphanet:85280)
Intellectual deficit, X-linked - seizures - psoriasis (Orphanet:3052)
Intellectual deficit, X-linked, Snyder type (Orphanet:3063)
Intellectual deficit, X-linked, Vitale type (Orphanet:85289)
Jackson-Weiss syndrome (Orphanet:1540)
Jacobsen syndrome (Orphanet:2308)
Kabuki syndrome (Orphanet:2322)
Kenny-Caffey syndrome (Orphanet:2333)
Koolen-De Vries syndrome (Orphanet:96169)
Langer mesomelic dysplasia (Orphanet:2632)
Langer-Giedion syndrome (Orphanet:502)
Lateral meningocele syndrome (Orphanet:2789)
Lathosterolosis (Orphanet:46059)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Leprechaunism (Orphanet:508)
Leukocyte adhesion deficiency (Orphanet:2968)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
MACS syndrome (Orphanet:217335)
Mandibuloacral dysplasia with type A lipodystrophy (Orphanet:90153)
Marfan syndrome (Orphanet:558)
Marfanoid habitus - intellectual deficit, autosomal recessive (Orphanet:2463)
Marshall syndrome (Orphanet:560)
McDonough syndrome (Orphanet:2471)
McKusick-Kaufman syndrome (Orphanet:2473)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Melhem-Fahl syndrome (Orphanet:2482)
Menkes disease (Orphanet:565)
Mesomelia-synostoses syndrome (Orphanet:2496)
Micro syndrome (Orphanet:2510)
Microcephaly - brachydactyly - kyphoscoliosis (Orphanet:3433)
Microcephaly - cardiac defect - lung malsegmentation (Orphanet:2516)
Microcephaly - deafness - intellectual deficit (Orphanet:2533)
Microcephaly - glomerulonephritis - marfanoid habitus (Orphanet:2172)
Microcephaly-cardiomyopathy syndrome (Orphanet:2515)
Microcephaly-microcornea syndrome, Seemanova type (Orphanet:2528)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Mitochondrial myopathy and sideroblastic anemia (Orphanet:2598)
Moebius syndrome (Orphanet:570)
Monosomy 5p (Orphanet:281)
Monosomy 9p (Orphanet:261112)
Mosaic trisomy 14 (Orphanet:1703)
Mosaic trisomy 8 (Orphanet:96061)
Mosaic trisomy 9 (Orphanet:99776)
Mowat-Wilson syndrome (Orphanet:2152)
Muckle-Wells syndrome (Orphanet:575)
Muenke syndrome (Orphanet:53271)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
Muscular dystrophy - white matter spongiosis (Orphanet:1877)
Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 (OMIM:600462)
Neonatal adrenoleukodystrophy (Orphanet:44)
Night blindness - skeletal anomalies - dysmorphism (Orphanet:1390)
Non-distal trisomy 10q (Orphanet:1695)
Non-distal trisomy 13q (Orphanet:1702)
Noonan syndrome (Orphanet:648)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Occipital horn syndrome (Orphanet:198)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
Oculocerebrofacial syndrome, Kaufman type (Orphanet:2707)
Oculocerebrorenal syndrome (Orphanet:534)
Oculofaciocardiodental syndrome (Orphanet:2712)
Oliver syndrome (Orphanet:2920)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 2 (Orphanet:2751)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Orofaciodigital syndrome type 8 (Orphanet:2755)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Otodental syndrome (Orphanet:2791)
Otofaciocervical syndrome (Orphanet:2792)
PEHO syndrome (Orphanet:2836)
Paraplegia - brachydactyly - cone-shaped epiphysis (Orphanet:2823)
Patterson-Stevenson-Fontaine syndrome (Orphanet:2439)
Perlman syndrome (Orphanet:2849)
Pfeiffer syndrome (Orphanet:710)
Pfeiffer syndrome type 1 (Orphanet:93258)
Pfeiffer syndrome type 2 (Orphanet:93259)
Pfeiffer syndrome type 3 (Orphanet:93260)
Pfeiffer-Palm-Teller syndrome (Orphanet:2871)
Phocomelia, Schinzel type (Orphanet:2879)
Polyvalvular heart disease syndrome (Orphanet:228410)
Prader-Willi syndrome (Orphanet:739)
Pseudoxanthoma elasticum (Orphanet:758)
Ptosis - strabismus - ectopic pupils (Orphanet:2999)
Pycnodysostosis (Orphanet:763)
Pyruvate dehydrogenase deficiency (Orphanet:765)
Qazi-Markouizos syndrome (Orphanet:3010)
RAPADILINO syndrome (Orphanet:3021)
Rabson-Mendenhall syndrome (Orphanet:769)
Radio-renal syndrome (Orphanet:3015)
Radio-ulnar synostosis - intellectual deficit - hypotonia (Orphanet:3270)
Ramon syndrome (Orphanet:3019)
Renal-genital-middle ear anomalies (Orphanet:1092)
Renpenning syndrome (Orphanet:3242)
Rhizomelic syndrome, Urbach type (Orphanet:3098)
Richieri Costa-Pereira syndrome (Orphanet:3102)
Ring chromosome 8 (Orphanet:1450)
Roberts syndrome (Orphanet:3103)
Rubinstein-Taybi syndrome (Orphanet:783)
SCARF syndrome (Orphanet:3134)
Say-Barber-Miller syndrome (Orphanet:3132)
Schilbach-Rott syndrome (Orphanet:2353)
Schwartz-Jampel syndrome (Orphanet:800)
Sheldon-Hall syndrome (Orphanet:1147)
Short stature - heart defect - craniofacial anomalies (Orphanet:1088)
Short stature - valvular heart disease - characteristic facies (Orphanet:2868)
Short stature - wormian bones - dextrocardia (Orphanet:2863)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Sotos syndrome (Orphanet:821)
Spastic diplegia, infantile type (Orphanet:1680)
Splenogonadal fusion - limb defects - micrognathia (Orphanet:2063)
Split hand - urinary anomalies - spina bifida (Orphanet:2437)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Syndromic X-linked intellectual deficit due to JARID1C mutation (Orphanet:85279)
Teebi-Shaltout syndrome (Orphanet:3291)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Temtamy syndrome (Orphanet:1777)
Thin ribs - tubular bones - dysmorphism (Orphanet:1506)
Toriello-Carey syndrome (Orphanet:3338)
Treacher-Collins syndrome (Orphanet:861)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Trigonocephaly - short stature - developmental delay (Orphanet:3369)
Trisomy 13 (Orphanet:3378)
Trisomy 17p (Orphanet:261290)
Trisomy 18 (Orphanet:3380)
Trisomy 20p (Orphanet:261318)
Trisomy 4p (Orphanet:1738)
Trisomy 8q (Orphanet:1752)
Ulbright-Hodes syndrome (Orphanet:3404)
Van Regemorter-Pierquin-Vamos syndrome (Orphanet:3419)
Van den Ende-Gupta syndrome (Orphanet:2460)
Velo-facial-skeletal syndrome (Orphanet:3424)
Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence (Orphanet:3201)
Vici syndrome (Orphanet:1493)
White forelock with malformations (Orphanet:2475)
Wolcott-Rallison syndrome (Orphanet:1667)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)
X-linked mandibulofacial dysostosis (Orphanet:1131)
Yunis-Varon syndrome (Orphanet:3472)
Zellweger syndrome (Orphanet:912)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)