Narrow naris
Symptom Information:
Symptom ID: | HPO:0009933 | |||||||
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) Abnormality of the nares(HPO:0005288) Narrow naris(HPO:0009933) MedDRA: |
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Database Frequency: | 16 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
12q14 microdeletion syndrome | (Orphanet:94063) |
8q22.1 microdeletion syndrome | (Orphanet:178303) |
Brachytelephalangy - dysmorphism - Kallmann syndrome | (Orphanet:1295) |
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis | (Orphanet:171839) |
Deafness with labyrinthine aplasia, microtia, and microdontia | (Orphanet:90024) |
Freeman-Sheldon syndrome | (Orphanet:2053) |
Gingival fibromatosis - facial dysmorphism | (Orphanet:2025) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
Maxillo-nasal dysplasia | (Orphanet:1248) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Phocomelia - ectrodactyly - deafness - sinus arrhythmia | (Orphanet:2878) |
ROBERTS SYNDROME | (OMIM:268300) |
Roberts syndrome | (Orphanet:3103) |
Trichodental syndrome | (Orphanet:3351) |