Abnormality of the nose

Symptom Information:

Symptom ID: HPO:0000366
Synonyms:
Nose and olfaction anomaly [Orphanet:8000]
Anomalies of nose and olfaction [Orphanet:8000]
Quality:
Cross references:
Orphanet:8000 "Anomalies of nose and olfaction" [Orphanet:8000]
Is a (Direct Parents):
HPO         Abnormality of procerus muscle
HPO         Neoplasm of the nose
HPO         Abnormality of nasalis muscle
HPO         Abnormal nasal base
HPO         Abnormality of nasal hair
HPO         Abnormality of the face
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)
MedDRA:
Database Frequency: 56 / 7739
Resource:

All diseases associated with this symptom:

17q11.2 microduplication syndrome (Orphanet:139474)
17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
8q21.11 microdeletion syndrome (Orphanet:284160)
AREDYLD syndrome (Orphanet:1133)
Acromelic frontonasal dysplasia (Orphanet:1827)
Alkaptonuria (Orphanet:56)
Anophthalmia plus syndrome (Orphanet:1104)
Arrhinia (Orphanet:1134)
Bifid nose (Orphanet:2695)
Bloom syndrome (Orphanet:125)
CODAS syndrome (Orphanet:1458)
Christianson syndrome (Orphanet:85278)
Cockayne syndrome (Orphanet:191)
Craniofrontonasal dysplasia (Orphanet:1520)
Craniosynostosis - cataract (Orphanet:1530)
Cutis laxa (Orphanet:209)
De Barsy syndrome (Orphanet:2962)
Diprosopia (Orphanet:1681)
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE (OMIM:614941)
Ectodermal dysplasia, tricho-odonto-onychial type (Orphanet:1818)
Epidermolysis bullosa simplex with pyloric atresia (Orphanet:158684)
FACES syndrome (Orphanet:1969)
Fabry disease (Orphanet:324)
Focal facial dermal dysplasia (Orphanet:79133)
Fraser syndrome (Orphanet:2052)
Fronto-facio-nasal dysostosis (Orphanet:1791)
Frontonasal dysplasia (Orphanet:250)
Frontonasal dysplasia with alopecia and genital anomaly (Orphanet:228390)
Granulomatosis with polyangiitis (Orphanet:900)
Holoprosencephaly (Orphanet:2162)
Hydrolethalus (Orphanet:2189)
Hypertelorism-microtia-facial clefting syndrome (Orphanet:2213)
Hypertrichosis (Orphanet:79365)
Hypospadias - hypertelorism - coloboma and deafness (Orphanet:157788)
Intellectual deficit - balding - patella luxation - acromicria (Orphanet:3041)
Marfanoid habitus - intellectual deficit, autosomal recessive (Orphanet:2463)
Mycophenolate mofetil embryopathy (Orphanet:268249)
Myotonia permanens (Orphanet:99735)
NOSE, ANOMALOUS SHAPE OF (OMIM:164000)
Neurofaciodigitorenal syndrome (Orphanet:2673)
Night blindness - skeletal anomalies - dysmorphism (Orphanet:1390)
Occipital horn syndrome (Orphanet:198)
Oculodentodigital dysplasia (Orphanet:2710)
Oculofaciocardiodental syndrome (Orphanet:2712)
Oculomaxillofacial dysostosis (Orphanet:1794)
Oculotrichoanal syndrome (Orphanet:2717)
Orofaciodigital syndrome type 2 (Orphanet:2751)
Pai syndrome (Orphanet:1993)
Relapsing polychondritis (Orphanet:728)
Rothmund-Thomson syndrome (Orphanet:2909)
Rothmund-Thomson syndrome type 2 (Orphanet:221016)
Solitary median maxillary central incisor syndrome (Orphanet:2286)
Syndactyly - telecanthus - anogenital and renal malformations (Orphanet:140952)
Trigonocephaly - bifid nose - acral anomalies (Orphanet:3368)
Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence (Orphanet:3201)
Waardenburg-Shah syndrome (Orphanet:897)