Prominent nasal bridge
Symptom Information:
Symptom ID: | HPO:0000426 | ||||||||||||
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) Prominent nasal bridge(HPO:0000426) MedDRA: |
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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) |