Abnormal nasal morphology

Symptom Information:

Symptom ID: HPO:0005105
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the nose
HPO         Proboscis
HPO         Fullness of paranasal tissue
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:
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)