Abnormality of the nasopharynx
Symptom Information:
| Symptom ID: | HPO:0001739 | ||||||
| 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 nasopharynx(HPO:0001739) Abnormality of the pharynx(HPO:0000600) Abnormality of the nasopharynx(HPO:0001739) MedDRA: |
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| Database Frequency: | 16 / 7739 | ||||||
| Resource: |
All diseases associated with this symptom:
| CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE | (OMIM:218400) |
| Craniometaphyseal dysplasia | (Orphanet:1522) |
| Crouzon disease | (Orphanet:207) |
| Distal myopathy with vocal cord weakness | (Orphanet:600) |
| ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
| EEC syndrome | (Orphanet:1896) |
| Hallermann-Streiff syndrome | (Orphanet:2108) |
| Moebius syndrome | (Orphanet:570) |
| OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
| Okihiro syndrome | (Orphanet:93293) |
| Osteoglophonic dwarfism | (Orphanet:2645) |
| Roifman syndrome | (Orphanet:353298) |
| Schinzel-Giedion syndrome | (Orphanet:798) |
| Solitary median maxillary central incisor syndrome | (Orphanet:2286) |
| VACTERL/VATER association | (Orphanet:887) |
| X-linked Opitz G/BBB syndrome | (Orphanet:306597) |