Thin bony cortex
Symptom Information:
Symptom ID: | HPO:0002753 | ||||
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 the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal bone structure(HPO:0003330) Abnormal cortical bone morphology(HPO:0003103) Thin bony cortex(HPO:0002753) MedDRA: |
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Database Frequency: | 16 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2 | (OMIM:615282) |
Dent disease type 1 | (Orphanet:93622) |
FACIOCARDIOMELIC SYNDROME | (OMIM:612731) |
Familial expansile osteolysis | (Orphanet:85195) |
Glaucoma - ectopia - microspherophakia - stiff joints - short stature | (Orphanet:2084) |
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE | (OMIM:300554) |
Hereditary hypophosphatemic rickets with hypercalciuria | (Orphanet:157215) |
Hypocalcemic vitamin D-dependent rickets | (Orphanet:289157) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
Proteus syndrome | (Orphanet:744) |
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A | (OMIM:264700) |
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B | (OMIM:600081) |
VITAMIN D-DEPENDENT RICKETS, TYPE 2A | (OMIM:277440) |
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR | (OMIM:600785) |
WEILL-MARCHESANI SYNDROME 1 | (OMIM:277600) |
Weill-Marchesani syndrome | (Orphanet:3449) |