Generalized osteosclerosis

Symptom Information:

Symptom ID: HPO:0005789
Synonyms:
Diffuse, symmetrical osteosclerosis [HPO:0005789]
Osteosclerosis, diffuse symmetrical [HPO:0005789]
Diffuse, symmetrical osteosclerosis [OMIM:Diffuse, symmetrical osteosclerosis]
Generalized osteosclerosis [OMIM:Generalized osteosclerosis]
Osteosclerosis, diffuse symmetrical [OMIM:Osteosclerosis, diffuse symmetrical]
Osteosclerosis, generalized [OMIM:Osteosclerosis, generalized]
Quality:
Cross references:
OMIM: "Diffuse, symmetrical osteosclerosis" [OMIM:Diffuse, symmetrical osteosclerosis]
OMIM: "Generalized osteosclerosis" [OMIM:Generalized osteosclerosis]
OMIM: "Osteosclerosis, diffuse symmetrical" [OMIM:Osteosclerosis, diffuse symmetrical]
OMIM: "Osteosclerosis, generalized" [OMIM:Osteosclerosis, generalized]
Is a (Direct Parents):
HPO         Increased 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)
                   Increased bone mineral density(HPO:0011001)
                      Generalized osteosclerosis(HPO:0005789)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Albers-Schönberg osteopetrosis (Orphanet:53)
Autosomal dominant osteopetrosis type 1 (Orphanet:2783)
Blue diaper syndrome (Orphanet:94086)
Chondrodysplasia, Blomstrand type (Orphanet:50945)
Desmosterolosis (Orphanet:35107)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
OSTEOMALACIA, SCLEROSING, WITH CEREBRAL CALCIFICATION (OMIM:259660)