Thickened cortex of long bones
Symptom Information:
Symptom ID: | HPO:0000935 | |||||||
Synonyms: |
|
|||||||
Quality: | ||||||||
Cross references: |
|
|||||||
Is a (Direct Parents): |
|
|||||||
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) Abnormality of long bone morphology(HPO:0011314) Thickened cortex of long bones(HPO:0000935) Abnormal bone structure(HPO:0003330) Abnormal cortical bone morphology(HPO:0003103) Thickened cortex of bones(HPO:0100039) Thickened cortex of long bones(HPO:0000935) MedDRA: |
|||||||
Database Frequency: | 8 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Kenny-Caffey syndrome | (Orphanet:93325) |
Autosomal dominant osteosclerosis, Worth type | (Orphanet:2790) |
HYPEROSTOSIS CORTICALIS GENERALISATA | (OMIM:239100) |
Hyperostosis corticalis generalisata | (Orphanet:3416) |
Kenny-Caffey syndrome | (Orphanet:2333) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
VAN BUCHEM DISEASE, TYPE 2 | (OMIM:607636) |