Narrow nasal bridge
Symptom Information:
Symptom ID: | HPO:0000446 | |||||||||
Synonyms: |
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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 nasal bridge(HPO:0000422) Narrow nasal bridge(HPO:0000446) MedDRA: |
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Database Frequency: | 29 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
19p13.12 microdeletion syndrome | (Orphanet:254346) |
Baller-Gerold syndrome | (Orphanet:1225) |
Conductive deafness - ptosis - skeletal anomalies | (Orphanet:3236) |
Dysostosis, Stanescu type | (Orphanet:1798) |
Ectodermal dysplasia - blindness | (Orphanet:1806) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Fibular aplasia - complex brachydactyly | (Orphanet:2639) |
Focal dermal hypoplasia | (Orphanet:2092) |
Fryns-Smeets-Thiry syndrome | (Orphanet:2058) |
Intellectual deficit - dysmorphism - hypogonadism - diabetes mellitus | (Orphanet:3044) |
Intellectual deficit - polydactyly - uncombable hair | (Orphanet:3082) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Kenny-Caffey syndrome | (Orphanet:2333) |
LUJAN-FRYNS SYNDROME | (OMIM:309520) |
Microbrachycephaly - ptosis - cleft lip | (Orphanet:2511) |
Microcephalic osteodysplastic dysplasia, Saul-Wilson type | (Orphanet:85172) |
Norrie disease | (Orphanet:649) |
OCULODENTODIGITAL DYSPLASIA | (OMIM:164200) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Prader-Willi syndrome | (Orphanet:739) |
Pseudoprogeria syndrome | (Orphanet:2985) |
RAPADILINO syndrome | (Orphanet:3021) |
Solitary median maxillary central incisor syndrome | (Orphanet:2286) |
Stoll-Alembik-Finck syndrome | (Orphanet:3200) |
Torg-Winchester syndrome | (Orphanet:3460) |
Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
Trichodental syndrome | (Orphanet:3351) |
Van den Ende-Gupta syndrome | (Orphanet:2460) |
Waardenburg syndrome type 3 | (Orphanet:896) |