Increased bone mineral density
Symptom Information:
Symptom ID: | HPO:0011001 | |||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): | ||||||||||||||||||||
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: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Bone disorders (excl congenital and fractures)(MedDRA:10005959) Bone disorders NEC(MedDRA:10027658) Increased bone mineral density(HPO:0011001) Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396) Non-site specific bone disorders congenital(MedDRA:10029509) Increased bone mineral density(HPO:0011001) 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) |
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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) |