Thin bony cortex

Symptom Information:

Symptom ID: HPO:0002753
Synonyms:
Thin cortices [HPO:0002753]
Thin bony cortex [OMIM:Thin bony cortex]
Thin cortices [OMIM:Thin cortices]
Thin cortex [OMIM:Thin cortex]
Quality:
Cross references:
OMIM: "Thin bony cortex" [OMIM:Thin bony cortex]
OMIM: "Thin cortices" [OMIM:Thin cortices]
OMIM: "Thin cortex" [OMIM:Thin cortex]
Is a (Direct Parents):
HPO         Abnormal cortical bone morphology
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:
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)