Generalized bone demineralization

Symptom Information:

Symptom ID: HPO:0006462
Synonyms:
Demineralisation [Orphanet:45090]
Decalcified structure (morphologic abnormality) [Orphanet:45090]
Demineralized structure (morphologic abnormality) [Orphanet:45090]
Decalcification [Orphanet:45090]
Generalized bone demineralization [OMIM:Generalized bone demineralization]
Osteoporosis/osteopenia/demineralisation/osteomalacia/rickets [Orphanet:45090]
Quality:
Cross references:
Orphanet:45090 "Osteoporosis/osteopenia/demineralisation/osteomalacia/rickets" [Orphanet:45090]
OMIM: "Generalized bone demineralization" [OMIM:Generalized bone demineralization]
UMLS:C0700185 "Decalcification" [Orphanet:45090]
Is a (Direct Parents):
Orphanet Osteopenia
Orphanet Abnormality of the skeletal system
HPO         Reduced bone mineral density
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)
                Abnormality of bone mineral density(HPO:0004348)
                   Reduced bone mineral density(HPO:0004349)
                      Generalized bone demineralization(HPO:0006462)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME (OMIM:215250)
CHST3-related skeletal dysplasia (Orphanet:263463)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Cystinosis (Orphanet:213)
Hemochromatosis type 2 (Orphanet:79230)
Menkes disease (Orphanet:565)
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR (OMIM:600785)
Werner syndrome (Orphanet:902)
Wilson disease (Orphanet:905)
Wolcott-Rallison syndrome (Orphanet:1667)