Anteverted nares

Symptom Information:

Symptom ID: HPO:0000463
Synonyms:
Anteverted nose [HPO:0000463]
Anteverted nostrils [HPO:0000463]
Nasal tip, upturned [HPO:0000463]
Nostrils anteverted [HPO:0000463]
Upturned nasal tip [HPO:0000463]
UPTURNED NASAL TIPS [HPO:0000463]
Upturned nose [HPO:0000463]
Anteverted nares [OMIM:Anteverted nares]
Anteverted nose [OMIM:Anteverted nose]
Anteverted nostrils [OMIM:Anteverted nostrils]
Nostrils anteverted [OMIM:Nostrils anteverted]
Upturned nasal tip [OMIM:Upturned nasal tip]
Upturned nasal tips [OMIM:Upturned nasal tips]
Upturned nose [OMIM:Upturned nose]
Anteverted nares/nostrils [Orphanet:8450]
Anteverted nares (96%) [OMIM:Anteverted nares (96%)]
Anteverted nares (in some patients) [OMIM:Anteverted nares (in some patients)]
Anteverted nares (some) [OMIM:Anteverted nares (some)]
Anteverted nostrils (in one family) [OMIM:Anteverted nostrils (in one family)]
Upturned nasal tip (in some patients) [OMIM:Upturned nasal tip (in some patients)]
Quality:
Cross references:
Orphanet:8450 "Anteverted nares/nostrils" [Orphanet:8450]
OMIM: "Anteverted nares" [OMIM:Anteverted nares]
OMIM: "Anteverted nose" [OMIM:Anteverted nose]
OMIM: "Anteverted nostrils" [OMIM:Anteverted nostrils]
OMIM: "Nostrils anteverted" [OMIM:Nostrils anteverted]
OMIM: "Upturned nasal tip" [OMIM:Upturned nasal tip]
OMIM: "Upturned nasal tips" [OMIM:Upturned nasal tips]
OMIM: "Upturned nose" [OMIM:Upturned nose]
OMIM: "Anteverted nares (96%)" [OMIM:Anteverted nares (96%)]
OMIM: "Anteverted nares (in some patients)" [OMIM:Anteverted nares (in some patients)]
OMIM: "Anteverted nares (some)" [OMIM:Anteverted nares (some)]
OMIM: "Anteverted nostrils (in one family)" [OMIM:Anteverted nostrils (in one family)]
OMIM: "Upturned nasal tip (in some patients)" [OMIM:Upturned nasal tip (in some patients)]
Is a (Direct Parents):
HPO         Abnormal nasal morphology
HPO         Abnormality of the nasal alae
Orphanet Abnormality of the nose
HPO         Abnormality of the nares
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 nares(HPO:0005288)
                      Anteverted nares(HPO:0000463)
                   Abnormality of the external nose(HPO:0010938)
                      Abnormality of the nasal alae(HPO:0000429)
                         Anteverted nares(HPO:0000463)
                   Abnormal nasal morphology(HPO:0005105)
                      Anteverted nares(HPO:0000463)
MedDRA:
Database Frequency: 305 / 7739
Resource:

All diseases associated with this symptom:

10q22.3q23.3 microdeletion syndrome (Orphanet:276413)
15q24 microdeletion syndrome (Orphanet:94065)
16p11.2p12.2 microdeletion syndrome (Orphanet:261211)
16p13.11 microdeletion syndrome (Orphanet:261236)
16q24.3 microdeletion syndrome (Orphanet:261250)
17q21.31 microduplication syndrome (Orphanet:217340)
19p13.12 microdeletion syndrome (Orphanet:254346)
1p36 deletion syndrome (Orphanet:1606)
1q41q42 microdeletion syndrome (Orphanet:250999)
2q32q33 microdeletion syndrome (Orphanet:251019)
2q37 microdeletion syndrome (Orphanet:1001)
3M syndrome (Orphanet:2616)
3q13 microdeletion syndrome (Orphanet:1621)
5q14.3 microdeletion syndrome (Orphanet:228384)
AARSKOG SYNDROME, AUTOSOMAL DOMINANT (OMIM:100050)
AARSKOG-SCOTT SYNDROME (OMIM:305400)
ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE (OMIM:614613)
AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA (OMIM:613623)
AICA-ribosiduria (Orphanet:250977)
Aarskog-Scott syndrome (Orphanet:915)
Ablepharon macrostomia syndrome (Orphanet:920)
Achondrogenesis (Orphanet:932)
Achondrogenesis type 1A (Orphanet:93299)
Achondrogenesis type 1B (Orphanet:93298)
Achondrogenesis type 2 (Orphanet:93296)
Achondroplasia (Orphanet:15)
Acrocraniofacial dysostosis (Orphanet:949)
Acrodysostosis (Orphanet:950)
Acrodysostosis with multiple hormone resistance (Orphanet:280651)
Acromicric dysplasia (Orphanet:969)
Acroosteolysis, dominant type (Orphanet:955)
Adenylosuccinate lyase deficiency (Orphanet:46)
Aicardi syndrome (Orphanet:50)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 (Orphanet:98791)
Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis (Orphanet:86818)
Aniridia - renal agenesis - psychomotor retardation (Orphanet:1064)
Antley-Bixler syndrome (Orphanet:83)
Arachnodactyly - abnormal ossification - intellectual deficit (Orphanet:1129)
Arthrogryposis multiplex congenita (Orphanet:1037)
Aspartylglucosaminuria (Orphanet:93)
Atkin-Flaitz syndrome (Orphanet:1193)
Atypical Rett syndrome (Orphanet:3095)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant spondylocostal dysostosis (Orphanet:1797)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive chorioretinopathy-microcephaly (Orphanet:2518)
Autosomal recessive cutis laxa type 2, classic type (Orphanet:357074)
Autosomal recessive cutis laxa type 2A (Orphanet:357058)
Autosomal recessive deafness-onychodystrophy syndrome (Orphanet:79500)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Autosomal recessive omodysplasia (Orphanet:93329)
Autosomal recessive spondylocostal dysostosis (Orphanet:2311)
Axial spondylometaphyseal dysplasia (Orphanet:168549)
BAINBRIDGE-ROPERS SYNDROME (OMIM:615485)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Baraitser-Winter syndrome (Orphanet:2995)
Barber-Say syndrome (Orphanet:1231)
Bardet-Biedl syndrome 17 (OMIM:615994)
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency (Orphanet:329255)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
Bone dysplasia, lethal Holmgren type (Orphanet:1842)
Brain malformation - congenital heart disease - postaxial polydactyly (Orphanet:75389)
C syndrome (Orphanet:1308)
CARDIOFACIOCUTANEOUS SYNDROME 2 (OMIM:615278)
CARPENTER SYNDROME 2 (OMIM:614976)
CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
CHROMOSOME 1p32-p31 DELETION SYNDROME (OMIM:613735)
CHROMOSOME 22q13 DUPLICATION SYNDROME (OMIM:615538)
CLARK-BARAITSER SYNDROME (OMIM:300602)
CODAS syndrome (Orphanet:1458)
COLD-INDUCED SWEATING SYNDROME 1 (OMIM:272430)
CORNELIA DE LANGE SYNDROME 1 (OMIM:122470)
CORNELIA DE LANGE SYNDROME 2 (OMIM:300590)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carey-Fineman-Ziter syndrome (Orphanet:1358)
Carpenter-Waziri syndrome (Orphanet:93973)
Cartilage-hair hypoplasia (Orphanet:175)
Cataract - aberrant oral frenula - growth delay (Orphanet:1373)
Cerebro-oculo-nasal syndrome (Orphanet:66625)
Cerebro-reno-digital syndrome (Orphanet:1396)
Chondrodysplasia, Blomstrand type (Orphanet:50945)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Cleft palate - short stature - vertebral anomalies (Orphanet:2015)
Coffin-Lowry syndrome (Orphanet:192)
Cold-induced sweating syndrome (Orphanet:157820)
Congenital intrauterine infection-like syndrome (Orphanet:1229)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
Connective tissue disorder due to lysyl hydroxylase-3 deficiency (Orphanet:300284)
Cooper-Jabs syndrome (Orphanet:1488)
Corneal anesthesia - deafness - intellectual deficit (Orphanet:1051)
Cornelia de Lange syndrome (Orphanet:199)
Costello syndrome (Orphanet:3071)
Crane-Heise syndrome (Orphanet:1512)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Craniolenticulosutural dysplasia (Orphanet:50814)
Craniomicromelic syndrome (Orphanet:1524)
Craniorhiny (Orphanet:157832)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Cutis laxa (Orphanet:209)
DEND syndrome (Orphanet:79134)
Deafness - onychodystrophy (Orphanet:3231)
Delayed speech - facial asymmetry - strabismus - ear lobe creases (Orphanet:3038)
Desbuquois syndrome (Orphanet:1425)
Desmosterolosis (Orphanet:35107)
Diaphragmatic defect - limb deficiency - skull defect (Orphanet:2141)
Dislocation of the hip - dysmorphism (Orphanet:2412)
Distal arthrogryposis type 5D (Orphanet:329457)
Distal monosomy 3p (Orphanet:1620)
Distal monosomy 6p (Orphanet:96125)
Distal trisomy 18q (Orphanet:1716)
Duane retraction syndrome (Orphanet:233)
Dysmorphism - multiple structural anomalies (Orphanet:1780)
Dysmorphism - short stature - deafness - disorder of sex development (Orphanet:2282)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 (OMIM:300672)
Edinburgh malformation syndrome (Orphanet:1895)
Embryofetopathy due to oral anticoagulant therapy (Orphanet:1914)
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria (Orphanet:1035)
Epilepsy telangiectasia (Orphanet:1951)
Epiphyseal dysplasia - hearing loss - dysmorphism (Orphanet:1825)
FACES syndrome (Orphanet:1969)
FACIAL PARESIS, HEREDITARY CONGENITAL, 3 (OMIM:614744)
FACIOCARDIOMELIC SYNDROME (OMIM:612731)
FACIOTHORACOGENITAL SYNDROME (OMIM:227320)
FEINGOLD SYNDROME 1 (OMIM:164280)
FIBROCHONDROGENESIS 1 (OMIM:228520)
FIBROCHONDROGENESIS 2 (OMIM:614524)
Familial intestinal malrotation - facial anomalies (Orphanet:2454)
Familial visceral myopathy (Orphanet:2604)
Feingold syndrome (Orphanet:1305)
Fetal Gaucher disease (Orphanet:85212)
Fetal alcohol syndrome (Orphanet:1915)
Fibrochondrogenesis (Orphanet:2021)
Free sialic acid storage disease, infantile form (Orphanet:309324)
Frontonasal dysplasia with alopecia and genital anomaly (Orphanet:228390)
Fryns syndrome (Orphanet:2059)
Fumaric aciduria (Orphanet:24)
GAPO syndrome (Orphanet:2067)
GELEOPHYSIC DYSPLASIA 1 (OMIM:231050)
Geleophysic dysplasia (Orphanet:2623)
Gómez-López-Hernández syndrome (Orphanet:1532)
HAJDU-CHENEY SYNDROME (OMIM:102500)
HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES (OMIM:613124)
Hall-Riggs syndrome (Orphanet:2107)
Heart defect - round face - congenital developmental delay (Orphanet:1355)
Hepatic fibrosis - renal cysts - intellectual deficit (Orphanet:2031)
Hirschsprung disease - nail hypoplasia - dysmorphism (Orphanet:2153)
Holmes-Gang syndrome (Orphanet:93970)
Holoprosencephaly (Orphanet:2162)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Hypertrichosis (Orphanet:79365)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Hypohidrotic ectodermal dysplasia (Orphanet:238468)
Hypomandibular faciocranial dysostosis (Orphanet:1790)
ICF syndrome (Orphanet:2268)
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2 (OMIM:614069)
Intellectual deficit - short stature - hypertelorism (Orphanet:3074)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
Intellectual deficit, X-linked - seizures - psoriasis (Orphanet:3052)
Intellectual deficit, X-linked, Wittwer type (Orphanet:85291)
Jacobsen syndrome (Orphanet:2308)
Joubert syndrome (Orphanet:475)
Joubert syndrome 1 (OMIM:213300)
Joubert syndrome 3 (OMIM:608629)
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)
Juberg-Marsidi syndrome (Orphanet:93972)
KAGAMI-OGATA SYNDROME (OMIM:608149)
KBG syndrome (Orphanet:2332)
Kleefstra syndrome (Orphanet:261494)
Kleefstra syndrome due to 9q34 microdeletion (Orphanet:96147)
Lathosterolosis (Orphanet:46059)
Leprechaunism (Orphanet:508)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
Lethal polymalformative syndrome, Boissel type (Orphanet:210144)
Leukocyte adhesion deficiency (Orphanet:2968)
Leukoencephalopathy - metaphyseal chondrodysplasia (Orphanet:83629)
Lichstenstein syndrome (Orphanet:2390)
MENTAL RETARDATION, X-LINKED 30 (OMIM:300558)
MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA (OMIM:608624)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 (OMIM:257300)
Mandibulofacial dysostosis - macroblepharon - macrostomia (Orphanet:357158)
Mandibulofacial dysostosis-microcephaly syndrome (Orphanet:79113)
Marden-Walker syndrome (Orphanet:2461)
Marshall syndrome (Orphanet:560)
Marshall-Smith syndrome (Orphanet:561)
Meckel syndrome, type 12 (OMIM:616258)
Metaphyseal acroscyphodysplasia (Orphanet:1240)
Micro syndrome (Orphanet:2510)
Microcephaly - facio-cardio-skeletal syndrome, Hadziselimovic type (Orphanet:217026)
Microcephaly - lymphedema - chorioretinopathy (Orphanet:2526)
Miller-Dieker syndrome (Orphanet:531)
Monosomy 9p (Orphanet:261112)
Mosaic trisomy 14 (Orphanet:1703)
Mosaic trisomy 8 (Orphanet:96061)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Mucolipidosis type 2 (Orphanet:576)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Mucopolysaccharidosis type 4 (Orphanet:582)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 (Orphanet:300496)
Multiple epiphyseal dysplasia (Orphanet:251)
Multiple osteochondromas (Orphanet:321)
Multiple sulfatase deficiency (Orphanet:585)
NOONAN SYNDROME 3 (OMIM:609942)
Neonatal adrenoleukodystrophy (Orphanet:44)
Neonatal hemochromatosis (Orphanet:446)
Non-progressive cerebellar ataxia with intellectual deficit (Orphanet:314647)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
Oculodentodigital dysplasia (Orphanet:2710)
Oculootodental syndrome (Orphanet:99806)
Okamoto syndrome (Orphanet:2729)
Opitz G/BBB syndrome (Orphanet:2745)
Opsismodysplasia (Orphanet:2746)
Orofaciodigital syndrome type 8 (Orphanet:2755)
Osteocraniostenosis (Orphanet:2763)
Osteoglophonic dwarfism (Orphanet:2645)
Otodental syndrome (Orphanet:2791)
Otofaciocervical syndrome (Orphanet:2792)
Otospondylomegaepiphyseal dysplasia (Orphanet:1427)
PEHO syndrome (Orphanet:2836)
PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER) (OMIM:614883)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
PEROXISOME BIOGENESIS DISORDER 2B (OMIM:202370)
PITUITARY HORMONE DEFICIENCY, COMBINED, 1 (OMIM:613038)
Pallister-Hall syndrome (Orphanet:672)
Perlman syndrome (Orphanet:2849)
Permanent neonatal diabetes mellitus (Orphanet:99885)
Peters-plus syndrome (Orphanet:709)
Pilodental dysplasia - refractive errors (Orphanet:2892)
Pitt-Hopkins syndrome (Orphanet:2896)
Polysyndactyly - cardiac malformation (Orphanet:2934)
Proteus syndrome (Orphanet:744)
Proteus-like syndrome (Orphanet:2969)
Ptosis - upper ocular movement limitation - absence of lacrimal punctum (Orphanet:228396)
Pyruvate dehydrogenase E1-alpha deficiency (Orphanet:79243)
RHINY (OMIM:180360)
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2 (OMIM:616331)
Rabson-Mendenhall syndrome (Orphanet:769)
Recombinant 8 syndrome (Orphanet:96167)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Retinitis pigmentosa (Orphanet:791)
Rhizomelic chondrodysplasia punctata type 2 (Orphanet:309796)
Ring chromosome 1 (Orphanet:1437)
Ring chromosome 8 (Orphanet:1450)
Roifman syndrome (Orphanet:353298)
SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES (OMIM:615789)
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL (OMIM:602613)
SPONASTRIME dysplasia (Orphanet:93357)
SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE (OMIM:613320)
STEVENSON-CAREY SYNDROME (OMIM:611961)
STICKLER SYNDROME, TYPE I (OMIM:108300)
Sanfilippo syndrome type D (Orphanet:79272)
Scalp-ear-nipple syndrome (Orphanet:2036)
Schinzel-Giedion syndrome (Orphanet:798)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Simpson-Golabi-Behmel syndrome type 2 (Orphanet:79022)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Solitary median maxillary central incisor syndrome (Orphanet:2286)
Sotos syndrome (Orphanet:821)
Spinocerebellar ataxia - dysmorphism (Orphanet:1185)
Spondylocarpotarsal synostosis (Orphanet:3275)
Spondyloepimetaphyseal dysplasia with multiple dislocations (Orphanet:93360)
Spondyloepiphyseal dysplasia, Cantu type (Orphanet:163654)
Spondylometaphyseal dysplasia, Golden type (Orphanet:168544)
Stickler syndrome (Orphanet:828)
Stickler syndrome type 2 (Orphanet:90654)
Stickler syndrome type 3 (Orphanet:166100)
Subaortic stenosis - short stature (Orphanet:3191)
Syndromic diarrhea (Orphanet:84064)
TARP syndrome (Orphanet:2886)
TEMPLE SYNDROME (OMIM:616222)
TENORIO SYNDROME (OMIM:616260)
THREE M SYNDROME 1 (OMIM:273750)
THREE M SYNDROME 2 (OMIM:612921)
THREE M SYNDROME 3 (OMIM:614205)
TMCO1 defect syndrome (Orphanet:228407)
TRICHOHEPATOENTERIC SYNDROME 1 (OMIM:222470)
TRICHOTHIODYSTROPHY, NONPHOTOSENSITIVE 1 (OMIM:234050)
Tetrasomy 12p (Orphanet:884)
Thrombocytopenia - Robin sequence (Orphanet:3323)
Thrombocytopenia - absent radius (Orphanet:3320)
Toriello-Carey syndrome (Orphanet:3338)
Toriello-Lacassie-Droste syndrome (Orphanet:3339)
Trisomy 20p (Orphanet:261318)
Williams syndrome (Orphanet:904)
X-linked Opitz G/BBB syndrome (Orphanet:306597)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)
Yunis-Varon syndrome (Orphanet:3472)
Zellweger syndrome (Orphanet:912)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)