Generalized bone demineralization
Symptom Information:
Symptom ID: | HPO:0006462 | ||||||
Synonyms: |
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Cross references: |
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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) Abnormality of bone mineral density(HPO:0004348) Reduced bone mineral density(HPO:0004349) Generalized bone demineralization(HPO:0006462) MedDRA: |
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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) |