Aplasia/Hypoplasia involving the nose
Symptom Information:
| Symptom ID: | HPO:0009924 | ||
| Synonyms: |
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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) Abnormal nasal morphology(HPO:0005105) Aplasia/Hypoplasia involving the nose(HPO:0009924) MedDRA: |
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| Database Frequency: | 18 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Acrodysostosis | (Orphanet:950) |
| Agnathia - holoprosencephaly - situs inversus | (Orphanet:990) |
| Arrhinia - choanal atresia - microphthalmia | (Orphanet:1135) |
| Baller-Gerold syndrome | (Orphanet:1225) |
| Chondrodysplasia, Blomstrand type | (Orphanet:50945) |
| Craniofacial-deafness-hand syndrome | (Orphanet:1529) |
| Desmosterolosis | (Orphanet:35107) |
| Fronto-facio-nasal dysostosis | (Orphanet:1791) |
| Frontonasal dysplasia with alopecia and genital anomaly | (Orphanet:228390) |
| Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
| Holoprosencephaly | (Orphanet:2162) |
| Holoprosencephaly - radial heart renal anomalies | (Orphanet:3186) |
| Laron syndrome | (Orphanet:633) |
| Laurin-Sandrow syndrome | (Orphanet:2378) |
| Marshall syndrome | (Orphanet:560) |
| Maxillo-nasal dysplasia | (Orphanet:1248) |
| Osteocraniostenosis | (Orphanet:2763) |
| Tetraamelia - multiple malformations | (Orphanet:3301) |