Prominent nasal bridge

Symptom Information:

Symptom ID: HPO:0000426
Synonyms:
Elevated nasal bridge [HPO:0000426]
High nasal bridge [HPO:0000426]
Prominent nasal root [HPO:0000426]
Elevated nasal bridge [OMIM:Elevated nasal bridge]
High nasal bridge [OMIM:High nasal bridge]
Prominent nasal bridge [OMIM:Prominent nasal bridge]
Prominent nasal root [OMIM:Prominent nasal root]
High nasal bridge [Orphanet:8330]
High nasal bridge (in 1 patient) [OMIM:High nasal bridge (in 1 patient)]
Nasal bridge high [OMIM:Nasal bridge high]
Prominent nasal bridge (in some patients) [OMIM:Prominent nasal bridge (in some patients)]
Prominent nasal root (in some patients) [OMIM:Prominent nasal root (in some patients)]
Quality:
Cross references:
Orphanet:8330 "High nasal bridge" [Orphanet:8330]
OMIM: "Elevated nasal bridge" [OMIM:Elevated nasal bridge]
OMIM: "High nasal bridge" [OMIM:High nasal bridge]
OMIM: "Prominent nasal bridge" [OMIM:Prominent nasal bridge]
OMIM: "Prominent nasal root" [OMIM:Prominent nasal root]
OMIM: "High nasal bridge (in 1 patient)" [OMIM:High nasal bridge (in 1 patient)]
OMIM: "Nasal bridge high" [OMIM:Nasal bridge high]
OMIM: "Prominent nasal bridge (in some patients)" [OMIM:Prominent nasal bridge (in some patients)]
OMIM: "Prominent nasal root (in some patients)" [OMIM:Prominent nasal root (in some patients)]
Is a (Direct Parents):
Orphanet Abnormality of the nose
HPO         Abnormality of the nasal bridge
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)
                      Prominent nasal bridge(HPO:0000426)
MedDRA:
Database Frequency: 121 / 7739
Resource:

All diseases associated with this symptom:

12q14 microdeletion syndrome (Orphanet:94063)
15q14 microdeletion syndrome (Orphanet:261190)
15q24 microdeletion syndrome (Orphanet:94065)
22q11.2 deletion syndrome (Orphanet:567)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2q32q33 microdeletion syndrome (Orphanet:251019)
3MC SYNDROME 2 (OMIM:265050)
3q29 microdeletion syndrome (Orphanet:65286)
6q16 deletion syndrome (Orphanet:171829)
ADULT syndrome (Orphanet:978)
AICA-ribosiduria (Orphanet:250977)
AREDYLD syndrome (Orphanet:1133)
Acrocraniofacial dysostosis (Orphanet:949)
Acrofacial dysostosis, Rodriguez type (Orphanet:1788)
Agenesis of the corpus callosum - intellectual deficit - coloboma - micrognathia (Orphanet:52055)
Antenatal multiminicore disease with arthrogryposis multiplex congenita (Orphanet:178148)
Aortic arch anomaly - peculiar facies - intellectual deficit (Orphanet:1110)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Baller-Gerold syndrome (Orphanet:1225)
Bardet-Biedl syndrome (Orphanet:110)
CEDNIK syndrome (Orphanet:66631)
CEREBROOCULOFACIOSKELETAL SYNDROME 1 (OMIM:214150)
CEREBROOCULOFACIOSKELETAL SYNDROME 4 (OMIM:610758)
CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
CK syndrome (Orphanet:251383)
COFS syndrome (Orphanet:1466)
CORNELIA DE LANGE SYNDROME 2 (OMIM:300590)
CORNELIA DE LANGE SYNDROME 3 (OMIM:610759)
CORNELIA DE LANGE SYNDROME 5 (OMIM:300882)
Cerebro-oculo-nasal syndrome (Orphanet:66625)
Choanal atresia - deafness - cardiac defects - dysmorphism (Orphanet:1200)
Cohen syndrome (Orphanet:193)
Cooks syndrome (Orphanet:1487)
Craniolenticulosutural dysplasia (Orphanet:50814)
Craniosynostosis - intracranial calcifications (Orphanet:52054)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal limb deficiencies - micrognathia syndrome (Orphanet:1307)
Distal monosomy 3p (Orphanet:1620)
Distal trisomy 15q (Orphanet:1707)
Distal trisomy 18q (Orphanet:1716)
Distal trisomy 6p (Orphanet:1745)
ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVEFACIAL FEATURES (OMIM:609944)
EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED (OMIM:130090)
FORSYTHE-WAKELING SYNDROME (OMIM:613606)
FRAXE intellectual deficit (Orphanet:100973)
FRONTOOCULAR SYNDROME (OMIM:605321)
Fabry disease (Orphanet:324)
Familial visceral myopathy (Orphanet:2604)
Filippi syndrome (Orphanet:3255)
Fryns-Smeets-Thiry syndrome (Orphanet:2058)
Genitopatellar syndrome (Orphanet:85201)
Glomerulonephritis - sparse hair - telangiectasis (Orphanet:2087)
Goldberg-Shprintzen megacolon syndrome (Orphanet:66629)
Grix-Blankenship-Peterson syndrome (Orphanet:2099)
Hypertelorism, Teebi type (Orphanet:1519)
Hypertrichosis cubiti - short stature (Orphanet:2220)
Intellectual deficit - myopathy - short stature - endocrine defect (Orphanet:3068)
Intellectual deficit, X-linked, Abidi type (Orphanet:85273)
Intellectual deficit, X-linked, Pai type (Orphanet:85322)
Isolated ATP synthase deficiency (Orphanet:254913)
Joubert syndrome (Orphanet:475)
Joubert syndrome 14 (OMIM:614424)
Joubert syndrome with hepatic defect (Orphanet:1454)
Joubert syndrome with ocular defect (Orphanet:220493)
Joubert syndrome with oculorenal defect (Orphanet:2318)
Joubert syndrome with orofaciodigital defect (Orphanet:2754)
Joubert syndrome with renal defect (Orphanet:220497)
Keipert syndrome (Orphanet:2662)
Koolen-De Vries syndrome (Orphanet:96169)
LUJAN-FRYNS SYNDROME (OMIM:309520)
Lissencephaly syndrome, Norman-Roberts type (Orphanet:89844)
Lowry-MacLean syndrome (Orphanet:2409)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 32 (OMIM:616268)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 (OMIM:611091)
MENTAL RETARDATION, X-LINKED, SYNDROMIC 14 (OMIM:300676)
MGAT2-CDG (Orphanet:79329)
MICROHYDRANENCEPHALY (OMIM:605013)
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1 (OMIM:604273)
MOVED TO 210600 (OMIM:608664)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Microcephalic primordial dwarfism due to ZNF335 deficiency (Orphanet:329228)
Microcephaly - brachydactyly - kyphoscoliosis (Orphanet:3433)
Microcephaly - facio-cardio-skeletal syndrome, Hadziselimovic type (Orphanet:217026)
Monosomy 13q14 (Orphanet:1587)
Mosaic trisomy 14 (Orphanet:1703)
Myhre syndrome (Orphanet:2588)
Nager syndrome (Orphanet:245)
Nance-Horan syndrome (Orphanet:627)
Neurofaciodigitorenal syndrome (Orphanet:2673)
Neurologic Waardenburg-Shah syndrome (Orphanet:163746)
Oculofaciocardiodental syndrome (Orphanet:2712)
Orofaciodigital syndrome type 8 (Orphanet:2755)
Otopalatodigital syndrome (Orphanet:669)
Pontocerebellar hypoplasia type 6 (Orphanet:166073)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
Primordial short stature - microdontia - opalescent and rootless teeth (Orphanet:46658)
Prominent glabella - microcephaly - hypogenitalism (Orphanet:2083)
Pseudoprogeria syndrome (Orphanet:2985)
Qazi-Markouizos syndrome (Orphanet:3010)
RUIJS-AALFS SYNDROME (OMIM:616200)
Radio-ulnar synostosis - intellectual deficit - hypotonia (Orphanet:3270)
SCARF syndrome (Orphanet:3134)
SECKEL SYNDROME 5 (OMIM:613823)
SHORT STATURE-OBESITY SYNDROME (OMIM:269870)
Say-Barber-Miller syndrome (Orphanet:3132)
Schwartz-Jampel syndrome (Orphanet:800)
Syndromic X-linked intellectual deficit due to JARID1C mutation (Orphanet:85279)
THAI SYMPHALANGISM SYNDROME (OMIM:608028)
Urban-Rogers-Meyer syndrome (Orphanet:3409)
Velo-facial-skeletal syndrome (Orphanet:3424)
WARBURG MICRO SYNDROME 2 (OMIM:614225)
WHISTLING FACE SYNDROME, RECESSIVE FORM (OMIM:277720)
Waardenburg syndrome (Orphanet:3440)
Waardenburg syndrome type 3 (Orphanet:896)
Waardenburg-Shah syndrome (Orphanet:897)
Woodhouse-Sakati syndrome (Orphanet:3464)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)
X-linked intellectual deficit, Najm type (Orphanet:163937)
X-linked lissencephaly with abnormal genitalia (Orphanet:452)
X-linked mandibulofacial dysostosis (Orphanet:1131)