Abnormality of connective tissue
Symptom Information:
| Symptom ID: | HPO:0003549 | ||||
| Synonyms: |
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| Cross references: |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of connective tissue(HPO:0003549) MedDRA: |
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| Database Frequency: | 22 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Angio-osteohypertrophic syndrome | (Orphanet:2346) |
| Autosomal agammaglobulinemia | (Orphanet:33110) |
| Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
| Caffey disease | (Orphanet:1310) |
| Dermatomyositis | (Orphanet:221) |
| Dissecting cellulitis of the scalp | (Orphanet:345) |
| Dracunculiasis | (Orphanet:231) |
| Eosinophilic fasciitis | (Orphanet:3165) |
| Felty syndrome | (Orphanet:47612) |
| Infantile myofibromatosis | (Orphanet:2591) |
| Isolated agammaglobulinemia | (Orphanet:229717) |
| Klippel-Trénaunay syndrome | (Orphanet:90308) |
| Legionellosis | (Orphanet:549) |
| Lipedema | (Orphanet:77243) |
| Localized lipodystrophy | (Orphanet:79088) |
| Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
| Nodular non-suppurative panniculitis | (Orphanet:33577) |
| Primary cutaneous lymphoma | (Orphanet:542) |
| Pseudoxanthoma elasticum | (Orphanet:758) |
| TRAPS syndrome | (Orphanet:32960) |
| Wells syndrome | (Orphanet:901) |
| X-linked agammaglobulinemia | (Orphanet:47) |