Anteverted nares
Symptom Information:
Symptom ID: | HPO:0000463 | ||||||||||||||||||||
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 external nose(HPO:0010938) Abnormality of the nasal alae(HPO:0000429) Anteverted nares(HPO:0000463) Abnormal nasal morphology(HPO:0005105) Anteverted nares(HPO:0000463) Abnormality of the nares(HPO:0005288) Anteverted nares(HPO:0000463) MedDRA: |
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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) |