Severe generalized osteoporosis
Symptom Information:
Symptom ID: | HPO:0005897 | ||||
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) Osteoporosis(HPO:0000939) Severe generalized osteoporosis(HPO:0005897) MedDRA: |
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Database Frequency: | 4 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III | (OMIM:210730) |
Nestor-Guillermo progeria syndrome | (Orphanet:280576) |
OSTEOGENESIS IMPERFECTA, TYPE III | (OMIM:259420) |
Osteogenesis imperfecta type 3 | (Orphanet:216812) |