Osteoporosis
Symptom Information:
Symptom ID: | HPO:0000939 | ||||||||||
Synonyms: |
|
||||||||||
Quality: | |||||||||||
Cross references: |
|
||||||||||
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) Reduced bone mineral density(HPO:0004349) Osteoporosis(HPO:0000939) MedDRA: |
||||||||||
Database Frequency: | 129 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
46,XX gonadal dysgenesis | (Orphanet:243) |
ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2 | (OMIM:615954) |
ACTH-independent macronodular adrenal hyperplasia | (Orphanet:189427) |
AMINO ACIDURIA WITH MENTAL DEFICIENCY, DWARFISM, MUSCULAR DYSTROPHY,OSTEOPOROSIS, AND ACIDOSIS | (OMIM:204730) |
ANALBUMINEMIA | (OMIM:616000) |
Albright hereditary osteodystrophy | (Orphanet:665) |
Aneurysm - osteoarthritis syndrome | (Orphanet:284984) |
Autosomal recessive limb-girdle muscular dystrophy type 2E | (Orphanet:119) |
BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 15 | (OMIM:613418) |
BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 18 | (OMIM:300910) |
BRUCK SYNDROME 1 | (OMIM:259450) |
Bruck syndrome | (Orphanet:2771) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
CEREBROOCULOFACIOSKELETAL SYNDROME 1 | (OMIM:214150) |
COCKAYNE SYNDROME B | (OMIM:133540) |
COFS syndrome | (Orphanet:1466) |
Cerebrotendinous xanthomatosis | (Orphanet:909) |
Classical homocystinuria | (Orphanet:394) |
Coats plus syndrome | (Orphanet:313838) |
Cockayne syndrome | (Orphanet:191) |
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis | (Orphanet:94062) |
Costello syndrome | (Orphanet:3071) |
Cranio-osteoarthropathy | (Orphanet:1525) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 1 | (OMIM:218330) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Cystinosis | (Orphanet:213) |
DESBUQUOIS DYSPLASIA 1 | (OMIM:251450) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 | (OMIM:613989) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3 | (OMIM:613990) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 | (OMIM:224230) |
Desbuquois syndrome | (Orphanet:1425) |
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome | (Orphanet:2229) |
Dominant hypophosphatemia with nephrolithiasis or osteoporosis | (Orphanet:244305) |
Dyskeratosis congenita | (Orphanet:1775) |
Ehlers-Danlos syndrome, kyphoscoliotic type | (Orphanet:1900) |
FORSYTHE-WAKELING SYNDROME | (OMIM:613606) |
Farber lipogranulomatosis | (Orphanet:333) |
Flynn-Aird syndrome | (Orphanet:2047) |
Frank-Ter Haar syndrome | (Orphanet:137834) |
Fucosidosis | (Orphanet:349) |
GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY | (OMIM:608278) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 3 | (Orphanet:77261) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Geroderma osteodysplastica | (Orphanet:2078) |
Glycogen storage disease due to glucose-6-phosphatase deficiency | (Orphanet:364) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
Goldblatt syndrome | (Orphanet:166272) |
HAJDU-CHENEY SYNDROME | (OMIM:102500) |
HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION | (OMIM:601979) |
HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA | (OMIM:615267) |
HYPOGONADOTROPIC HYPOGONADISM 19 WITH OR WITHOUT ANOSMIA | (OMIM:615269) |
HYPOGONADOTROPIC HYPOGONADISM 20 WITH OR WITHOUT ANOSMIA | (OMIM:615270) |
HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA | (OMIM:615271) |
HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA | (OMIM:610628) |
Hall-Riggs syndrome | (Orphanet:2107) |
Hemochromatosis type 2 | (Orphanet:79230) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
IMMUNODEFICIENCY 12 | (OMIM:615468) |
Idiopathic juvenile osteoporosis | (Orphanet:85193) |
Intellectual deficit - cataracts - calcified pinnae - myopathy | (Orphanet:3042) |
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy | (Orphanet:2958) |
Intellectual deficit, X-linked, Snyder type | (Orphanet:3063) |
Isolated glycerol kinase deficiency | (Orphanet:408) |
Juvenile Paget disease | (Orphanet:2801) |
Juvenile hyaline fibromatosis | (Orphanet:2028) |
LOEYS-DIETZ SYNDROME 2 | (OMIM:610168) |
Larsen-like syndrome, B3GAT3 type | (Orphanet:284139) |
Lathosterolosis | (Orphanet:46059) |
Lichstenstein syndrome | (Orphanet:2390) |
Lysinuric protein intolerance | (Orphanet:470) |
MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGEDAPPEARANCE | (OMIM:248010) |
MACS syndrome | (Orphanet:217335) |
MELAS | (Orphanet:550) |
MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM | (OMIM:616033) |
MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY | (OMIM:259600) |
Mandibular hypoplasia-deafness-progeroid syndrome | (Orphanet:363649) |
Menkes disease | (Orphanet:565) |
Micro syndrome | (Orphanet:2510) |
Mucopolysaccharidosis type 4A | (Orphanet:309297) |
Mucopolysaccharidosis type 4B | (Orphanet:309310) |
NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1 | (OMIM:612286) |
NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2 | (OMIM:612287) |
NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY | (OMIM:256720) |
Nestor-Guillermo progeria syndrome | (Orphanet:280576) |
Niemann-Pick disease type A | (Orphanet:77292) |
OSTEOGENESIS IMPERFECTA, TYPE XII | (OMIM:613849) |
OSTEOGENESIS IMPERFECTA, TYPE XIII | (OMIM:614856) |
OSTEOPOROSIS | (OMIM:166710) |
OVARIAN DYSGENESIS 1 | (OMIM:233300) |
Occipital horn syndrome | (Orphanet:198) |
Osteoporosis - oculocutaneous hypopigmentation syndrome | (Orphanet:2786) |
Osteoporosis - pseudoglioma | (Orphanet:2788) |
PEROXISOME BIOGENESIS DISORDER 3B | (OMIM:266510) |
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 | (OMIM:610489) |
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2 | (OMIM:610475) |
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4 | (OMIM:615830) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 2E | (OMIM:615851) |
PREMATURE AGING SYNDROME, OKAMOTO TYPE | (OMIM:601811) |
PREMATURE OVARIAN FAILURE 2B | (OMIM:300604) |
Perrault Syndrome | (Orphanet:2855) |
Prader-Willi syndrome | (Orphanet:739) |
Primary pigmented nodular adrenocortical disease | (Orphanet:189439) |
Progressive pseudorheumatoid arthropathy of childhood | (Orphanet:1159) |
Propionic acidemia | (Orphanet:35) |
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia | (Orphanet:3390) |
Pseudohypoparathyroidism type 1A | (Orphanet:79443) |
Pseudohypoparathyroidism type 1C | (Orphanet:79444) |
Pseudopseudohypoparathyroidism | (Orphanet:79445) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Singleton-Merten dysplasia | (Orphanet:85191) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
TMEM165-CDG | (Orphanet:314667) |
Torg-Winchester syndrome | (Orphanet:3460) |
Urban-Rogers-Meyer syndrome | (Orphanet:3409) |
WARBURG MICRO SYNDROME 1 | (OMIM:600118) |
Werner syndrome | (Orphanet:902) |
Williams syndrome | (Orphanet:904) |
Wilson disease | (Orphanet:905) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |