Increased bone mineral density

Symptom Information:

Symptom ID: HPO:0011001
Synonyms:
Increased bone density [HPO:0011001]
Osteosclerosis [HPO:0011001]
Osteosclerosis of bones [HPO:0011001]
Osteopetrosis [Orphanet:45120]
Osteosclerosis [Orphanet:45120]
Osteosclerosis (disorder) [Orphanet:45120]
Increased bone density [OMIM:Increased bone density]
Increased bone mineral density [OMIM:Increased bone mineral density]
Osteosclerosis [OMIM:Osteosclerosis]
Osteosclerosis/osteopetrosis/bone condensation [Orphanet:45120]
Osteosclerosis [MedDRA:10031298]
Vertebral sclerosis [MedDRA:10031298]
Subchondral osteosclerosis [MedDRA:10031298]
Increased bone mineral density (in some patients) [OMIM:Increased bone mineral density (in some patients)]
Osteopetrosis (in severe cases) [OMIM:Osteopetrosis (in severe cases)]
Osteosclerosis (lesions mainly affect diaphyses of long bones, hands, feet, and pelvis although epiphyses may also be affected) [OMIM:Osteosclerosis (lesions mainly affect diaphyses of long bones, hands, feet, and pelvis although epiphyses may also be affected)]
Bone compression [Orphanet:45120]
Osteopetrosis [MedDRA:10031280]
Bone density increased [MedDRA:10057864]
Quality:
Cross references:
HPO:0011002 "Osteopetrosis" [Orphanet:45120]
Orphanet:45120 "Osteosclerosis/osteopetrosis/bone condensation" [Orphanet:45120]
OMIM: "Increased bone density" [OMIM:Increased bone density]
OMIM: "Increased bone mineral density" [OMIM:Increased bone mineral density]
OMIM: "Osteosclerosis" [OMIM:Osteosclerosis]
OMIM: "Increased bone mineral density (in some patients)" [OMIM:Increased bone mineral density (in some patients)]
OMIM: "Osteopetrosis (in severe cases)" [OMIM:Osteopetrosis (in severe cases)]
OMIM: "Osteosclerosis (lesions mainly affect diaphyses of long bones, hands, feet, and pelvis although epiphyses may also be affected)" [OMIM:Osteosclerosis (lesions mainly affect diaphyses of long bones, hands, feet, and pelvis although epiphyses may also be affected)]
UMLS:C0029464 "Osteosclerosis" [Orphanet:45120]
Is a (Direct Parents):
HPO         Abnormality of bone mineral density
Orphanet Abnormality of the skeletal system
MedDRA Musculoskeletal and soft tissue imaging procedures
MedDRA Bone disorders NEC
MedDRA Non-site specific bone disorders congenital
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)
MedDRA:
Investigations(MedDRA:10022891)
    Musculoskeletal and soft tissue investigations (excl enzyme tests)(MedDRA:10028387)
       Musculoskeletal and soft tissue imaging procedures(MedDRA:10028386)
          Increased bone mineral density(HPO:0011001)
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396)
       Non-site specific bone disorders congenital(MedDRA:10029509)
          Increased bone mineral density(HPO:0011001)
    Bone disorders (excl congenital and fractures)(MedDRA:10005959)
       Bone disorders NEC(MedDRA:10027658)
          Increased bone mineral density(HPO:0011001)
Database Frequency: 78 / 7739
Resource:

All diseases associated with this symptom:

AXIAL OSTEOMALACIA (OMIM:109130)
Adamantinoma (Orphanet:55881)
Aggressive systemic mastocytosis (Orphanet:98850)
Albers-Schönberg osteopetrosis (Orphanet:53)
Autosomal dominant Kenny-Caffey syndrome (Orphanet:93325)
Autosomal dominant osteosclerosis, Worth type (Orphanet:2790)
Autosomal recessive hypophosphatemic rickets (Orphanet:289176)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Beemer-Ertbruggen syndrome (Orphanet:1237)
Buschke-Ollendorff syndrome (Orphanet:1306)
CHARGE syndrome (Orphanet:138)
CLEIDOCRANIAL DYSPLASIA (OMIM:119600)
CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT (OMIM:122860)
Camurati-Engelmann disease (Orphanet:1328)
Chondrodysplasia, Blomstrand type (Orphanet:50945)
Chronic recurrent multifocal osteomyelitis (Orphanet:324964)
Cleidocranial dysplasia (Orphanet:1452)
Craniometaphyseal dysplasia (Orphanet:1522)
Cutaneous mastocytosis (Orphanet:66646)
Dacryocystitis - osteopoikilosis (Orphanet:1562)
Dentin dysplasia (Orphanet:1653)
Desmosterolosis (Orphanet:35107)
Diastrophic dwarfism (Orphanet:628)
Dysosteosclerosis (Orphanet:1782)
Dysostosis, Stanescu type (Orphanet:1798)
Dysplastic cortical hyperostosis (Orphanet:2204)
Erdheim-Chester disease (Orphanet:35687)
Fried syndrome (Orphanet:85335)
Gaucher disease (Orphanet:355)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 3 (Orphanet:77261)
Ghosal hematodiaphyseal dysplasia (Orphanet:1802)
Grix-Blankenship-Peterson syndrome (Orphanet:2099)
HYPEROSTOSIS CORTICALIS GENERALISATA (OMIM:239100)
HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE, 1 (OMIM:241520)
Hashimoto-Pritzker syndrome (Orphanet:99872)
Hereditary sensory and autonomic neuropathy type 4 (Orphanet:642)
Hyperostosis corticalis generalisata (Orphanet:3416)
Isolated osteopoikilosis (Orphanet:166119)
Kaler-Garrity-Stern syndrome (Orphanet:2324)
Kenny-Caffey syndrome (Orphanet:2333)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
Leukocyte adhesion deficiency type III (Orphanet:99844)
METAPHYSEAL MODELING ABNORMALITY, SKIN LESIONS, AND SPASTIC PARAPLEGIA (OMIM:250500)
Melorheostosis (Orphanet:2485)
Melorheostosis with osteopoikilosis (Orphanet:1879)
Metaphyseal chondrodysplasia, Jansen type (Orphanet:33067)
OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE (OMIM:602475)
OSTEOGENESIS IMPERFECTA, TYPE XIII (OMIM:614856)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2 (OMIM:259710)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3 (OMIM:259730)
OSTEOSCLEROSIS WITH ICHTHYOSIS AND FRACTURES (OMIM:166740)
Osteomesopyknosis (Orphanet:2777)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Osteopetrosis (Orphanet:2781)
Osteopetrosis with renal tubular acidosis (Orphanet:2785)
Osteosclerosis - developmental delay - craniosynostosis (Orphanet:178377)
Osteosclerosis - ichthyosis - premature ovarian failure (Orphanet:75325)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 1 (Orphanet:90650)
Otopalatodigital syndrome type 2 (Orphanet:90652)
POEMS syndrome (Orphanet:2905)
Primary hyperoxaluria (Orphanet:416)
Primary hyperoxaluria type 1 (Orphanet:93598)
Pycnodysostosis (Orphanet:763)
Pyknoachondrogenesis (Orphanet:3003)
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2 (OMIM:616331)
SAPHO syndrome (Orphanet:793)
Sanjad-Sakati syndrome (Orphanet:2323)
Schnitzler syndrome (Orphanet:37748)
Schwartz-Jampel syndrome (Orphanet:800)
Sclerosteosis (Orphanet:3152)
Systemic mastocytosis (Orphanet:2467)
TOOTH AGENESIS, SELECTIVE, 6 (OMIM:613097)
Tricho-dento-osseous syndrome (Orphanet:3352)
Werner syndrome (Orphanet:902)
Williams syndrome (Orphanet:904)