Abnormality of the nasal tip
Symptom Information:
| Symptom ID: | HPO:0000436 | ||
| 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 external nose(HPO:0010938) Abnormality of the nasal tip(HPO:0000436) MedDRA: |
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| Database Frequency: | 18 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Alar cartilages hypoplasia - coloboma - telecanthus | (Orphanet:2007) |
| Arthrogryposis multiplex congenita - whistling face | (Orphanet:1150) |
| Baraitser-Winter syndrome | (Orphanet:2995) |
| Bilateral renal agenesis | (Orphanet:1848) |
| Branchio-oculo-facial syndrome | (Orphanet:1297) |
| Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis | (Orphanet:171839) |
| Gonadal dysgenesis, XY type - associated anomalies | (Orphanet:1770) |
| Holoprosencephaly | (Orphanet:2162) |
| Hypoplastic tibiae - postaxial polydactyly | (Orphanet:3332) |
| Kabuki syndrome | (Orphanet:2322) |
| Laurin-Sandrow syndrome | (Orphanet:2378) |
| Maxillo-nasal dysplasia | (Orphanet:1248) |
| Non-rhizomelic chondrodysplasia punctata | (Orphanet:176) |
| Omphalocele syndrome, Shprintzen-Goldberg type | (Orphanet:3164) |
| Peters-plus syndrome | (Orphanet:709) |
| Short stature - wormian bones - dextrocardia | (Orphanet:2863) |
| Thymic-renal-anal-lung dysplasia | (Orphanet:3326) |
| Zimmermann-Laband syndrome | (Orphanet:3473) |