Severe generalized osteoporosis

Symptom Information:

Symptom ID: HPO:0005897
Synonyms:
Severe, generalized osteoporosis [HPO:0005897]
Severe osteoporosis [OMIM:Severe osteoporosis]
Severe, generalized osteoporosis [OMIM:Severe, generalized osteoporosis]
Osteoporosis, severe [OMIM:Osteoporosis, severe]
Quality:
Cross references:
OMIM: "Severe osteoporosis" [OMIM:Severe osteoporosis]
OMIM: "Severe, generalized osteoporosis" [OMIM:Severe, generalized osteoporosis]
OMIM: "Osteoporosis, severe" [OMIM:Osteoporosis, severe]
Is a (Direct Parents):
HPO         Osteoporosis
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:
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)