Abnormal nasal morphology
Symptom Information:
Symptom ID: | HPO:0005105 | ||||||
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) Abnormal nasal morphology(HPO:0005105) MedDRA: |
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Database Frequency: | 114 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
14q12 microdeletion syndrome | (Orphanet:261144) |
15q13.3 microdeletion syndrome | (Orphanet:199318) |
16p11.2p12.2 microdeletion syndrome | (Orphanet:261211) |
17q23.1q23.2 microdeletion syndrome | (Orphanet:261279) |
1q21.1 microdeletion syndrome | (Orphanet:250989) |
22q11.2 deletion syndrome | (Orphanet:567) |
22q11.2 microduplication syndrome | (Orphanet:1727) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
2q31.1 microdeletion syndrome | (Orphanet:251014) |
3M syndrome | (Orphanet:2616) |
4q21 microdeletion syndrome | (Orphanet:238750) |
6q16 deletion syndrome | (Orphanet:171829) |
AREDYLD syndrome | (Orphanet:1133) |
Ablepharon macrostomia syndrome | (Orphanet:920) |
Achalasia - microcephaly | (Orphanet:929) |
Acro-fronto-facio-nasal dysostosis | (Orphanet:1784) |
Acrofacial dysostosis, Palagonia type | (Orphanet:1787) |
Acromegaloid facial appearance syndrome | (Orphanet:965) |
Acromicric dysplasia | (Orphanet:969) |
Alagille syndrome | (Orphanet:52) |
Alopecia - contractures - dwarfism - intellectual deficit | (Orphanet:1005) |
Alopecia-intellectual deficit syndrome | (Orphanet:2850) |
Atkin-Flaitz syndrome | (Orphanet:1193) |
Autosomal recessive distal osteolysis syndrome | (Orphanet:2776) |
Baraitser-Winter syndrome | (Orphanet:2995) |
Barber-Say syndrome | (Orphanet:1231) |
Beemer-Ertbruggen syndrome | (Orphanet:1237) |
Blepharonasofacial malformation syndrome | (Orphanet:1252) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
Blepharophimosis-intellectual deficit syndrome, SBBYS type | (Orphanet:3047) |
Bowen-Conradi syndrome | (Orphanet:1270) |
Brachymorphism - onychodysplasia - dysphalangism | (Orphanet:1292) |
COFS syndrome | (Orphanet:1466) |
Cernunnos-XLF deficiency | (Orphanet:169079) |
Choanal atresia - deafness - cardiac defects - dysmorphism | (Orphanet:1200) |
Christianson syndrome | (Orphanet:85278) |
Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
Deafness - genital anomalies - metacarpal and metatarsal synostosis | (Orphanet:3224) |
Deafness with labyrinthine aplasia, microtia, and microdontia | (Orphanet:90024) |
Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
Distal monosomy 7q36 | (Orphanet:1636) |
Dysmorphism - multiple structural anomalies | (Orphanet:1780) |
Dysostosis, Stanescu type | (Orphanet:1798) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Familial osteodysplasia, Anderson type | (Orphanet:2769) |
Flat face - microstomia - ear anomaly | (Orphanet:1968) |
Floating-Harbor syndrome | (Orphanet:2044) |
Freeman-Sheldon syndrome | (Orphanet:2053) |
Genitopatellar syndrome | (Orphanet:85201) |
Grix-Blankenship-Peterson syndrome | (Orphanet:2099) |
Hall-Riggs syndrome | (Orphanet:2107) |
Hamel cerebro-palato-cardiac syndrome | (Orphanet:93946) |
Harrod syndrome | (Orphanet:2115) |
Hennekam-Beemer syndrome | (Orphanet:2135) |
Hernandez-Aguirre Negrete syndrome | (Orphanet:2139) |
Hirsutism - skeletal dysplasia - intellectual deficit | (Orphanet:2156) |
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly | (Orphanet:2180) |
Hydrocephaly - low insertion umbilicus | (Orphanet:2184) |
Intellectual deficit - dysmorphism - hypogonadism - diabetes mellitus | (Orphanet:3044) |
Intellectual deficit, Wolff type | (Orphanet:3080) |
Intellectual deficit, X-linked - hypotonia - facial dysmorphism - aggressive behavior | (Orphanet:85329) |
Intellectual deficit, X-linked, Shashi type | (Orphanet:85286) |
Intellectual deficit, X-linked, Vitale type | (Orphanet:85289) |
Kaler-Garrity-Stern syndrome | (Orphanet:2324) |
Kapur-Toriello syndrome | (Orphanet:2328) |
Koolen-De Vries syndrome | (Orphanet:96169) |
LIG4 syndrome | (Orphanet:99812) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Langer-Giedion syndrome | (Orphanet:502) |
Lathosterolosis | (Orphanet:46059) |
Laurin-Sandrow syndrome | (Orphanet:2378) |
Marfanoid habitus - intellectual deficit, autosomal recessive | (Orphanet:2463) |
McDonough syndrome | (Orphanet:2471) |
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus | (Orphanet:83473) |
Mesomelia-synostoses syndrome | (Orphanet:2496) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Monosomy 22q13 | (Orphanet:48652) |
Mosaic trisomy 8 | (Orphanet:96061) |
Mosaic trisomy 9 | (Orphanet:99776) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Mucolipidosis type 4 | (Orphanet:578) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Multiple epiphyseal dysplasia, Lowry type | (Orphanet:166016) |
Nager syndrome | (Orphanet:245) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Nance-Horan syndrome | (Orphanet:627) |
Neuroectodermal syndrome, Johnson type | (Orphanet:2316) |
Nijmegen breakage syndrome | (Orphanet:647) |
Oculo-palato-cerebral syndrome | (Orphanet:2714) |
Orofaciodigital syndrome type 2 | (Orphanet:2751) |
Orofaciodigital syndrome type 3 | (Orphanet:2752) |
Paraplegia - intellectual deficit - hyperkeratosis | (Orphanet:2824) |
Paternal 20q13.2q13.3 microdeletion syndrome | (Orphanet:261304) |
Phocomelia - ectrodactyly - deafness - sinus arrhythmia | (Orphanet:2878) |
Pilotto syndrome | (Orphanet:2894) |
Polysyndactyly - cardiac malformation | (Orphanet:2934) |
Polyvalvular heart disease syndrome | (Orphanet:228410) |
Preaxial polydactyly - colobomata - intellectual deficit | (Orphanet:2921) |
Radio-ulnar synostosis - intellectual deficit - hypotonia | (Orphanet:3270) |
Renpenning syndrome | (Orphanet:3242) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Sheldon-Hall syndrome | (Orphanet:1147) |
Teebi-Shaltout syndrome | (Orphanet:3291) |
Telecanthus - hypertelorism - strabismus - pes cavus | (Orphanet:3293) |
Tetralogy of Fallot | (Orphanet:3303) |
Torg-Winchester syndrome | (Orphanet:3460) |
Trichorhinophalangeal syndrome type 1 and 3 | (Orphanet:77258) |
Trigonocephaly - bifid nose - acral anomalies | (Orphanet:3368) |
Trisomy 17p | (Orphanet:261290) |
Trisomy 9p | (Orphanet:236) |
Williams syndrome | (Orphanet:904) |
Xq27.3q28 duplication syndrome | (Orphanet:261483) |
Zimmermann-Laband syndrome | (Orphanet:3473) |