High, narrow palate
Symptom Information:
Symptom ID: | HPO:0002705 | |||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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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) High palate(HPO:0000218) High, narrow palate(HPO:0002705) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Gastrointestinal tract disorders congenital(MedDRA:10018018) Palate disorders congenital(MedDRA:10033530) High, narrow palate(HPO:0002705) |
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Database Frequency: | 308 / 7739 | |||||||||||||||||||||||
Resource: |
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) |
HOLOPROSENCEPHALY 5 | (OMIM:609637) |
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) |
MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES | (OMIM:607597) |
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) |
SIMOSA CRANIOFACIAL SYNDROME | (OMIM:182150) |
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE | (OMIM:614066) |
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) |
TETRAAMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES | (OMIM:273390) |
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) |
VITILIGO, PROGRESSIVE, WITH MENTAL RETARDATION AND URETHRAL DUPLICATION | (OMIM:277465) |
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) |