Bone cyst
Symptom Information:
| Symptom ID: | HPO:0012062 | ||
| Synonyms: |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal bone structure(HPO:0003330) Bone cyst(HPO:0012062) MedDRA: |
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| Database Frequency: | 19 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| 17q11 microdeletion syndrome | (Orphanet:97685) |
| 17q11.2 microduplication syndrome | (Orphanet:139474) |
| Adamantinoma | (Orphanet:55881) |
| Alveolar echinococcosis | (Orphanet:284) |
| Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
| Cerebral gigantism - jaw cysts | (Orphanet:2081) |
| Cowden syndrome | (Orphanet:201) |
| Encephalocraniocutaneous lipomatosis | (Orphanet:2396) |
| Flynn-Aird syndrome | (Orphanet:2047) |
| Gorlin syndrome | (Orphanet:377) |
| Hydatidosis | (Orphanet:400) |
| Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
| Infantile myofibromatosis | (Orphanet:2591) |
| Intellectual deficit - cataracts - calcified pinnae - myopathy | (Orphanet:3042) |
| Nasu-Hakola disease | (Orphanet:2770) |
| Nephropathy - deafness - hyperparathyroidism | (Orphanet:2668) |
| SARCOIDOSIS, SUSCEPTIBILITY TO, 1 | (OMIM:181000) |
| Sarcoidosis | (Orphanet:797) |
| Trisomy 8q | (Orphanet:1752) |