Abnormality of the nose
Symptom Information:
Symptom ID: | HPO:0000366 | ||||||||||||
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) MedDRA: |
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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) |