Wide nasal bridge
Symptom Information:
Symptom ID: | HPO:0000431 | |||||||||||||||||||||||||||||
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 nose(HPO:0000366) Abnormality of the nasal bridge(HPO:0000422) Wide nasal bridge(HPO:0000431) MedDRA: |
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Database Frequency: | 290 / 7739 | |||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
1p36 deletion syndrome | (Orphanet:1606) |
20p12.3 microdeletion syndrome | (Orphanet:261295) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
3C syndrome | (Orphanet:7) |
3MC SYNDROME 2 | (OMIM:265050) |
3q29 microduplication | (Orphanet:251038) |
5p13 microduplication syndrome | (Orphanet:329802) |
6q25 microdeletion syndrome | (Orphanet:251056) |
8q12 microduplication syndrome | (Orphanet:228399) |
8q21.11 microdeletion syndrome | (Orphanet:284160) |
8q22.1 microdeletion syndrome | (Orphanet:178303) |
AARSKOG SYNDROME, AUTOSOMAL DOMINANT | (OMIM:100050) |
AARSKOG-SCOTT SYNDROME | (OMIM:305400) |
ALG3-CDG | (Orphanet:79321) |
AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM | (OMIM:104350) |
ARTHROGRYPOSIS, DISTAL, TYPE 2A | (OMIM:193700) |
AXENFELD-RIEGER SYNDROME, TYPE 1 | (OMIM:180500) |
AXENFELD-RIEGER SYNDROME, TYPE 2 | (OMIM:601499) |
Aarskog-Scott syndrome | (Orphanet:915) |
Acro-cardio-facial syndrome | (Orphanet:2008) |
Acro-fronto-facio-nasal dysostosis | (Orphanet:1784) |
Acrocallosal syndrome | (Orphanet:36) |
Acrofacial dysostosis, Rodriguez type | (Orphanet:1788) |
Acroosteolysis, dominant type | (Orphanet:955) |
Alar cartilages hypoplasia - coloboma - telecanthus | (Orphanet:2007) |
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 | (Orphanet:98791) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Atrioventricular defect - blepharophimosis -radial defects | (Orphanet:1352) |
Autosomal dominant Opitz G/BBB syndrome | (Orphanet:306588) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal dominant spondylocostal dysostosis | (Orphanet:1797) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive deafness-onychodystrophy syndrome | (Orphanet:79500) |
Autosomal recessive omodysplasia | (Orphanet:93329) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Axenfeld-Rieger syndrome | (Orphanet:782) |
BARAITSER-WINTER SYNDROME 1 | (OMIM:243310) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
Baraitser-Winter syndrome | (Orphanet:2995) |
Beemer-Ertbruggen syndrome | (Orphanet:1237) |
Blepharophimosis - epicanthus inversus - ptosis | (Orphanet:126) |
Blepharophimosis - ptosis - esotropia - syndactyly - short stature | (Orphanet:2057) |
Blepharophimosis-intellectual deficit syndrome, MKB type | (Orphanet:293707) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
Bohring-Opitz syndrome | (Orphanet:97297) |
Boomerang dysplasia | (Orphanet:1263) |
Brachydactyly - preaxial hallux varus | (Orphanet:1278) |
Brachymorphism - onychodysplasia - dysphalangism | (Orphanet:1292) |
Branchio-skeleto-genital syndrome | (Orphanet:1299) |
C syndrome | (Orphanet:1308) |
CARPENTER SYNDROME 2 | (OMIM:614976) |
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION | (OMIM:601088) |
CEDNIK syndrome | (Orphanet:66631) |
CHROMOSOME 16q22 DELETION SYNDROME | (OMIM:614541) |
CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME | (OMIM:613603) |
CLN10 disease | (Orphanet:228337) |
COFS syndrome | (Orphanet:1466) |
CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTALDELAY | (OMIM:616266) |
CORNELIA DE LANGE SYNDROME 4 | (OMIM:614701) |
CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT | (OMIM:122860) |
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE | (OMIM:218400) |
Carpenter-Waziri syndrome | (Orphanet:93973) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Cerebro-facio-articular syndrome | (Orphanet:314679) |
Chondrodysplasia with joint dislocations, gPAPP type | (Orphanet:280586) |
Chudley-Lowry-Hoar syndrome | (Orphanet:93971) |
Combined immunodeficiency with facio-oculo-skeletal anomalies | (Orphanet:221139) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
Congenital brain dysgenesis due to glutamine synthetase deficiency | (Orphanet:71278) |
Congenital lactic acidosis, Saguenay-Lac-St. Jean type | (Orphanet:70472) |
Congenital neuronal ceroid lipofuscinosis | (Orphanet:168486) |
Congenital pulmonary lymphangiectasia | (Orphanet:2414) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
Craniodiaphyseal dysplasia | (Orphanet:1513) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 1 | (OMIM:218330) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Craniofaciofrontodigital syndrome | (Orphanet:363705) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
Craniolenticulosutural dysplasia | (Orphanet:50814) |
Craniometaphyseal dysplasia | (Orphanet:1522) |
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies | (Orphanet:221145) |
Cystic fibrosis - gastritis - megaloblastic anemia | (Orphanet:2575) |
Dahlberg-Borer-Newcomer syndrome | (Orphanet:1563) |
Dandy-Walker malformation - postaxial polydactyly | (Orphanet:1566) |
De Barsy syndrome | (Orphanet:2962) |
Deafness - intellectual deficit, Martin-Probst type | (Orphanet:85321) |
Deafness with labyrinthine aplasia, microtia, and microdontia | (Orphanet:90024) |
Deafness-craniofacial syndrome | (Orphanet:3241) |
Dislocation of the hip - dysmorphism | (Orphanet:2412) |
Distal monosomy 10q | (Orphanet:96148) |
Distal monosomy 15q | (Orphanet:1596) |
Distal monosomy 9p | (Orphanet:1642) |
Duane retraction syndrome | (Orphanet:233) |
Dubowitz syndrome | (Orphanet:235) |
Dyssegmental dysplasia, Silverman-Handmaker type | (Orphanet:1865) |
ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY | (OMIM:600906) |
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1 | (OMIM:130070) |
Ehlers-Danlos syndrome, progeroid type | (Orphanet:75496) |
Endocrine-cerebro-osteodysplasia syndrome | (Orphanet:199332) |
Epimetaphyseal skeletal dysplasia | (Orphanet:1819) |
FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS | (OMIM:227255) |
FANCONI ANEMIA, COMPLEMENTATION GROUP L | (OMIM:614083) |
FEINGOLD SYNDROME 1 | (OMIM:164280) |
FG SYNDROME 4 | (OMIM:300422) |
Faciocardiorenal syndrome | (Orphanet:1973) |
Fallot complex - intellectual deficit - growth delay | (Orphanet:3304) |
Familial benign copper deficiency | (Orphanet:1551) |
Feingold syndrome | (Orphanet:1305) |
Fibulo-ulnar hypoplasia - renal anomalies | (Orphanet:2256) |
Filippi syndrome | (Orphanet:3255) |
Flat face - microstomia - ear anomaly | (Orphanet:1968) |
Floating-Harbor syndrome | (Orphanet:2044) |
Fraser syndrome | (Orphanet:2052) |
Freeman-Sheldon syndrome | (Orphanet:2053) |
Frontometaphyseal dysplasia | (Orphanet:1826) |
Frontonasal dysplasia | (Orphanet:250) |
Frontonasal dysplasia with alopecia and genital anomaly | (Orphanet:228390) |
Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome | (Orphanet:306542) |
Fryns syndrome | (Orphanet:2059) |
Genito-palato-cardiac syndrome | (Orphanet:2075) |
Glomerulonephritis - sparse hair - telangiectasis | (Orphanet:2087) |
Goldberg-Shprintzen megacolon syndrome | (Orphanet:66629) |
Gorlin syndrome | (Orphanet:377) |
Greig cephalopolysyndactyly syndrome | (Orphanet:380) |
Growth delay due to insulin-like growth factor I resistance | (Orphanet:73273) |
HELSMOORTEL-VAN DER AA SYNDROME | (OMIM:615873) |
HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT | (OMIM:235830) |
HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES | (OMIM:236410) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 | (OMIM:239300) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2 | (OMIM:614749) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4 | (OMIM:615716) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 5 | (OMIM:616025) |
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES | (OMIM:614684) |
Hall-Riggs syndrome | (Orphanet:2107) |
Hennekam syndrome | (Orphanet:2136) |
Hennekam-Beemer syndrome | (Orphanet:2135) |
Hereditary orotic aciduria | (Orphanet:30) |
Hermansky-Pudlak syndrome with neutropenia | (Orphanet:183678) |
Hirsutism - skeletal dysplasia - intellectual deficit | (Orphanet:2156) |
Histidinuria - renal tubular defect | (Orphanet:2158) |
Holmes-Gang syndrome | (Orphanet:93970) |
Hurler syndrome | (Orphanet:93473) |
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly | (Orphanet:2180) |
Hyperphosphatasia-intellectual deficiency syndrome | (Orphanet:247262) |
Hypertelorism, Teebi type | (Orphanet:1519) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Hypoglossia - hypodactyly | (Orphanet:989) |
IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES | (OMIM:615966) |
Imperforate oropharynx - costo vetebral anomalies | (Orphanet:2759) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Intellectual deficit, X-linked - seizures - psoriasis | (Orphanet:3052) |
Isolated trigonocephaly | (Orphanet:3366) |
Joubert syndrome 10 | (OMIM:300804) |
Joubert syndrome 3 | (OMIM:608629) |
Joubert syndrome with ocular defect | (Orphanet:220493) |
Juberg-Marsidi syndrome | (Orphanet:93972) |
Jung-Wolff-Back-Stahl syndrome | (Orphanet:2321) |
KAHRIZI SYNDROME | (OMIM:612713) |
Kabuki syndrome | (Orphanet:2322) |
Koolen-De Vries syndrome | (Orphanet:96169) |
LIG4 syndrome | (Orphanet:99812) |
Langer-Giedion syndrome | (Orphanet:502) |
Lathosterolosis | (Orphanet:46059) |
Leukocyte adhesion deficiency | (Orphanet:2968) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13 | (OMIM:613192) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15 | (OMIM:614202) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 45 | (OMIM:615979) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 | (OMIM:611091) |
MICROPHTHALMIA, SYNDROMIC 12 | (OMIM:615524) |
MICROPHTHALMIA, SYNDROMIC 9 | (OMIM:601186) |
MOMO syndrome | (Orphanet:2563) |
Mandibulofacial dysostosis - macroblepharon - macrostomia | (Orphanet:357158) |
Matthew-Wood syndrome | (Orphanet:2470) |
Meckel syndrome, type 12 | (OMIM:616258) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
Metaphyseal acroscyphodysplasia | (Orphanet:1240) |
Micro syndrome | (Orphanet:2510) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Miller-Dieker syndrome | (Orphanet:531) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Monosomy 18p | (Orphanet:1598) |
Monosomy 22q13 | (Orphanet:48652) |
Monosomy 5p | (Orphanet:281) |
Monosomy 9p | (Orphanet:261112) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Mucopolysaccharidosis type 2, attenuated form | (Orphanet:217093) |
Mulibrey nanism | (Orphanet:2576) |
Mullerian derivatives - lymphangiectasia - polydactyly | (Orphanet:1655) |
Multicentric carpo-tarsal osteolysis with or without nephropathy | (Orphanet:2774) |
Nasal dermoid cyst | (Orphanet:141103) |
Nasopalpebral lipoma - coloboma - telecanthus | (Orphanet:2399) |
Neonatal adrenoleukodystrophy | (Orphanet:44) |
Neurological conditions associated with aminoacylase 1 deficiency | (Orphanet:137754) |
Non-distal monosomy 10q | (Orphanet:1581) |
Oculomaxillofacial dysostosis | (Orphanet:1794) |
Oculoosteocutaneous syndrome | (Orphanet:2713) |
Omodysplasia | (Orphanet:2733) |
Omphalocele syndrome, Shprintzen-Goldberg type | (Orphanet:3164) |
Opitz G/BBB syndrome | (Orphanet:2745) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Orofaciodigital syndrome type 2 | (Orphanet:2751) |
Orofaciodigital syndrome type 8 | (Orphanet:2755) |
Osteocraniostenosis | (Orphanet:2763) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
Otopalatodigital syndrome type 1 | (Orphanet:90650) |
PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER) | (OMIM:614886) |
PEROXISOME BIOGENESIS DISORDER 1B | (OMIM:601539) |
PEROXISOME BIOGENESIS DISORDER 2B | (OMIM:202370) |
POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY | (OMIM:611087) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 10 | (OMIM:615803) |
Perlman syndrome | (Orphanet:2849) |
Peroxisomal acyl-CoA oxidase deficiency | (Orphanet:2971) |
Pfeiffer syndrome | (Orphanet:710) |
Phocomelia, Schinzel type | (Orphanet:2879) |
Piebaldism | (Orphanet:2884) |
Pilodental dysplasia - refractive errors | (Orphanet:2892) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Pontocerebellar hypoplasia type 7 | (Orphanet:284339) |
Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |
Potocki-Shaffer syndrome | (Orphanet:52022) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
Qazi-Markouizos syndrome | (Orphanet:3010) |
ROBERTS SYNDROME | (OMIM:268300) |
Renier-Gabreels-Jasper syndrome | (Orphanet:93975) |
Renpenning syndrome | (Orphanet:3242) |
Retinitis pigmentosa | (Orphanet:791) |
Rhizomelic chondrodysplasia punctata type 2 | (Orphanet:309796) |
Ring chromosome 1 | (Orphanet:1437) |
Ring chromosome 6 | (Orphanet:1448) |
Roberts syndrome | (Orphanet:3103) |
Rubinstein-Taybi syndrome | (Orphanet:783) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
SCARF syndrome | (Orphanet:3134) |
SHORT syndrome | (Orphanet:3163) |
SIMOSA CRANIOFACIAL SYNDROME | (OMIM:182150) |
SLC35A2-CDG | (Orphanet:356961) |
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE | (OMIM:614066) |
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE | (OMIM:613744) |
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES | (OMIM:600093) |
STEEL SYNDROME | (OMIM:615155) |
Sclerosteosis | (Orphanet:3152) |
Sheldon-Hall syndrome | (Orphanet:1147) |
Short stature - heart defect - craniofacial anomalies | (Orphanet:1088) |
Short stature - wormian bones - dextrocardia | (Orphanet:2863) |
Sialidosis type 1 | (Orphanet:812) |
Sialuria | (Orphanet:3166) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Skeletal dysplasia - intellectual deficit | (Orphanet:1436) |
Smith-Fineman-Myers syndrome | (Orphanet:93974) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Smith-Magenis syndrome | (Orphanet:819) |
Spondyloepiphyseal dysplasia, Cantu type | (Orphanet:163654) |
Spondylometaphyseal dysplasia, Golden type | (Orphanet:168544) |
Subaortic stenosis - short stature | (Orphanet:3191) |
TARP syndrome | (Orphanet:2886) |
THAI SYMPHALANGISM SYNDROME | (OMIM:608028) |
TMCO1 defect syndrome | (Orphanet:228407) |
TRISOMY 18-LIKE SYNDROME | (OMIM:601161) |
Tetrasomy 12p | (Orphanet:884) |
Thrombocytopenia - Robin sequence | (Orphanet:3323) |
Timothy syndrome | (Orphanet:65283) |
Toriello-Lacassie-Droste syndrome | (Orphanet:3339) |
Treacher-Collins syndrome | (Orphanet:861) |
Trigonocephaly - short stature - developmental delay | (Orphanet:3369) |
Trisomy 12p | (Orphanet:1699) |
Trisomy 8q | (Orphanet:1752) |
VAN MALDERGEM SYNDROME 1 | (OMIM:601390) |
VAN MALDERGEM SYNDROME 2 | (OMIM:615546) |
VERHEIJ SYNDROME | (OMIM:615583) |
Velo-facial-skeletal syndrome | (Orphanet:3424) |
W syndrome | (Orphanet:2804) |
WAARDENBURG SYNDROME, TYPE 2A | (OMIM:193510) |
WARBURG MICRO SYNDROME 4 | (OMIM:615663) |
Waardenburg syndrome | (Orphanet:3440) |
Waardenburg syndrome type 1 | (Orphanet:894) |
Waardenburg syndrome type 2 | (Orphanet:895) |
White matter hypoplasia - corpus callosum agenesis - intellectual deficit | (Orphanet:3207) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
Wrinkly skin syndrome | (Orphanet:2834) |
X-linked Opitz G/BBB syndrome | (Orphanet:306597) |
X-linked intellectual deficit - hypotonic face | (Orphanet:73220) |
X-linked intellectual deficit, Najm type | (Orphanet:163937) |
X-linked lissencephaly with abnormal genitalia | (Orphanet:452) |
Zechi-Ceide syndrome | (Orphanet:217017) |
Zellweger-like syndrome without peroxisomal anomalies | (Orphanet:50812) |
Zimmermann-Laband syndrome | (Orphanet:3473) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |
Zunich-Kaye syndrome | (Orphanet:3474) |