Osteoporosis

Symptom Information:

Symptom ID: HPO:0000939
Synonyms:
Generalized osteoporosis [HPO:0000939]
Ostoporosis [Orphanet:45090]
Generalized osteoporosis [OMIM:Generalized osteoporosis]
Osteoporosis [OMIM:Osteoporosis]
Osteoporosis/osteopenia/demineralisation/osteomalacia/rickets [Orphanet:45090]
Generalized osteoporosis (in some patients) [OMIM:Generalized osteoporosis (in some patients)]
Osteoporosis (70% of patients) [OMIM:Osteoporosis (70% of patients)]
Osteoporosis (classic feature) [OMIM:Osteoporosis (classic feature)]
Osteoporosis (in some patients) [OMIM:Osteoporosis (in some patients)]
Osteoporosis (onset in childhood) [OMIM:Osteoporosis (onset in childhood)]
Quality:
Cross references:
Orphanet:45090 "Osteoporosis/osteopenia/demineralisation/osteomalacia/rickets" [Orphanet:45090]
OMIM: "Generalized osteoporosis" [OMIM:Generalized osteoporosis]
OMIM: "Osteoporosis" [OMIM:Osteoporosis]
OMIM: "Generalized osteoporosis (in some patients)" [OMIM:Generalized osteoporosis (in some patients)]
OMIM: "Osteoporosis (70% of patients)" [OMIM:Osteoporosis (70% of patients)]
OMIM: "Osteoporosis (classic feature)" [OMIM:Osteoporosis (classic feature)]
OMIM: "Osteoporosis (in some patients)" [OMIM:Osteoporosis (in some patients)]
OMIM: "Osteoporosis (onset in childhood)" [OMIM:Osteoporosis (onset in childhood)]
UMLS:C0029456 "Osteoporosis" [HPO:0000939]
Is a (Direct Parents):
HPO         Generalized osteoporosis
HPO         Reduced bone mineral density
Orphanet Abnormality of the skeletal system
Orphanet Osteopenia
HPO         Localized 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)
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)