Osteopenia

Symptom Information:

Symptom ID: HPO:0000938
Synonyms:
Decreased bone mineral density [HPO:0000938]
Generalized osteopenia [HPO:0000938]
Osteopenia (disorder) [Orphanet:45090]
Osteopenia (morphologic abnormality) [Orphanet:45090]
Osteopenia [Orphanet:45090]
Decreased bone mineral density [OMIM:Decreased bone mineral density]
Generalized osteopenia [OMIM:Generalized osteopenia]
Osteopenia [OMIM:Osteopenia]
Osteoporosis/osteopenia/demineralisation/osteomalacia/rickets [Orphanet:45090]
Bone loss [Orphanet:45090]
Bone loss [MedDRA:10065687]
Bone loss in jaw [MedDRA:10065687]
Osteopenia [MedDRA:10049088]
Osteopaenia [MedDRA:10049088]
Osteopaenia periarticular [MedDRA:10049088]
Osteopenia periarticular [MedDRA:10049088]
Decreased bone mineral density (BMD) [OMIM:Decreased bone mineral density (BMD)]
Osteopenia (in some patients) [OMIM:Osteopenia (in some patients)]
Osteopenia (late-onset) [OMIM:Osteopenia (late-onset)]
Osteopenia (reported in 2 patients) [OMIM:Osteopenia (reported in 2 patients)]
Osteopenia, generalized [OMIM:Osteopenia, generalized]
Periarticular osteopenia [OMIM:Periarticular osteopenia]
Quality:
Cross references:
Orphanet:45090 "Osteoporosis/osteopenia/demineralisation/osteomalacia/rickets" [Orphanet:45090]
OMIM: "Decreased bone mineral density" [OMIM:Decreased bone mineral density]
OMIM: "Generalized osteopenia" [OMIM:Generalized osteopenia]
OMIM: "Osteopenia" [OMIM:Osteopenia]
OMIM: "Decreased bone mineral density (BMD)" [OMIM:Decreased bone mineral density (BMD)]
OMIM: "Osteopenia (in some patients)" [OMIM:Osteopenia (in some patients)]
OMIM: "Osteopenia (late-onset)" [OMIM:Osteopenia (late-onset)]
OMIM: "Osteopenia (reported in 2 patients)" [OMIM:Osteopenia (reported in 2 patients)]
OMIM: "Osteopenia, generalized" [OMIM:Osteopenia, generalized]
OMIM: "Periarticular osteopenia" [OMIM:Periarticular osteopenia]
UMLS:C0029453 "Osteopenia" [Orphanet:45090]
Is a (Direct Parents):
HPO         Reduced bone mineral density
Orphanet Abnormality of the skeletal system
MedDRA Bone disorders NEC
MedDRA Metabolic bone disorders
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)
                      Osteopenia(HPO:0000938)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Bone disorders (excl congenital and fractures)(MedDRA:10005959)
       Metabolic bone disorders(MedDRA:10027425)
          Osteopenia(HPO:0000938)
       Bone disorders NEC(MedDRA:10027658)
          Osteopenia(HPO:0000938)
Database Frequency: 138 / 7739
Resource:

All diseases associated with this symptom:

46,XY complete gonadal dysgenesis (Orphanet:242)
ACTH-independent macronodular adrenal hyperplasia (Orphanet:189427)
Acro-osteolysis-keloid-like lesions-premature aging syndrome (Orphanet:363665)
Alpha-N-acetylgalactosaminidase deficiency (Orphanet:3137)
Alpha-N-acetylgalactosaminidase deficiency type 1 (Orphanet:79279)
Alpha-N-acetylgalactosaminidase deficiency type 3 (Orphanet:79281)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Atypical Gaucher disease due to saposin C deficiency (Orphanet:309252)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal recessive cutis laxa type 2B (Orphanet:357064)
BARTTER SYNDROME, ANTENATAL, TYPE 1 (OMIM:601678)
BARTTER SYNDROME, ANTENATAL, TYPE 2 (OMIM:241200)
BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 18 (OMIM:300910)
BRUCK SYNDROME 2 (OMIM:609220)
Barth syndrome (Orphanet:111)
Bartter syndrome (Orphanet:112)
Bifunctional enzyme deficiency (Orphanet:300)
Brachyolmia type 1, Hobaek type (Orphanet:93301)
CANDLE syndrome (Orphanet:325004)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURALHEARING LOSS, AND SKELETAL DYSPLASIA (OMIM:616007)
COG1-CDG (Orphanet:263508)
COLE-CARPENTER SYNDROME 2 (OMIM:616294)
Camptodactyly syndrome, Guadalajara type 2 (Orphanet:1326)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Central diabetes insipidus (Orphanet:178029)
Cerebro-facio-articular syndrome (Orphanet:314679)
Coats plus syndrome (Orphanet:313838)
Cole-Carpenter syndrome (Orphanet:2050)
Combined immunodeficiency with facio-oculo-skeletal anomalies (Orphanet:221139)
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome (Orphanet:1369)
Congenital contractural arachnodactyly (Orphanet:115)
Congenital erythropoietic porphyria (Orphanet:79277)
Connective tissue disorder due to lysyl hydroxylase-3 deficiency (Orphanet:300284)
Costello syndrome (Orphanet:3071)
Cranio-osteoarthropathy (Orphanet:1525)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
Craniolenticulosutural dysplasia (Orphanet:50814)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Cystinosis (Orphanet:213)
DIABETES INSIPIDUS, NEUROHYPOPHYSEAL (OMIM:125700)
Diaphyseal medullary stenosis - bone malignancy (Orphanet:85182)
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome (Orphanet:2229)
Dominant hypophosphatemia with nephrolithiasis or osteoporosis (Orphanet:244305)
Dysosteosclerosis (Orphanet:1782)
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1 (OMIM:130070)
EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE (OMIM:615923)
ESTROGEN RESISTANCE (OMIM:615363)
EXUDATIVE VITREORETINOPATHY 4 (OMIM:601813)
Ehlers-Danlos syndrome type 7A (Orphanet:99875)
Ehlers-Danlos syndrome type 7B (Orphanet:99876)
Ehlers-Danlos syndrome, arthrochalasic type (Orphanet:1899)
Ehlers-Danlos syndrome, dermatosparaxis type (Orphanet:1901)
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type (Orphanet:300179)
Ehlers-Danlos syndrome, progeroid type (Orphanet:75496)
Ehlers-Danlos syndrome, spondylocheirodysplastic type (Orphanet:157965)
FACIOCARDIOMELIC SYNDROME (OMIM:612731)
FANCONI RENOTUBULAR SYNDROME 2 (OMIM:613388)
Frank-Ter Haar syndrome (Orphanet:137834)
Free sialic acid storage disease, infantile form (Orphanet:309324)
GELEOPHYSIC DYSPLASIA 1 (OMIM:231050)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Geleophysic dysplasia (Orphanet:2623)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Geroderma osteodysplastica (Orphanet:2078)
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)
Glycogen storage disease due to hepatic glycogen synthase deficiency (Orphanet:2089)
Gnathodiaphyseal dysplasia (Orphanet:53697)
Growth delay due to insulin-like growth factor type 1 deficiency (Orphanet:73272)
HAJDU-CHENEY SYNDROME (OMIM:102500)
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 8 WITH OR WITHOUT ANOSMIA (OMIM:614837)
Hemochromatosis type 2 (Orphanet:79230)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
IMMUNODEFICIENCY 31C (OMIM:614162)
Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome (Orphanet:369837)
JMP syndrome (Orphanet:324999)
Juvenile hyaline fibromatosis (Orphanet:2028)
Kaler-Garrity-Stern syndrome (Orphanet:2324)
Kallmann syndrome (Orphanet:478)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Linear nevus sebaceus syndrome (Orphanet:2612)
Lipodystrophy - intellectual deficit - deafness (Orphanet:50811)
MGAT2-CDG (Orphanet:79329)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Menkes disease (Orphanet:565)
Metaphyseal chondrodysplasia, Jansen type (Orphanet:33067)
Mucolipidosis type 2 (Orphanet:576)
Multicentric carpo-tarsal osteolysis with or without nephropathy (Orphanet:2774)
NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1 (OMIM:612286)
NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2 (OMIM:612287)
Nakajo-Nishimura syndrome (Orphanet:2615)
OSTEOGENESIS IMPERFECTA, TYPE V (OMIM:610967)
OSTEOGENESIS IMPERFECTA, TYPE VII (OMIM:610682)
OSTEOGENESIS IMPERFECTA, TYPE VIII (OMIM:610915)
OSTEOGENESIS IMPERFECTA, TYPE X (OMIM:613848)
OSTEOGENESIS IMPERFECTA, TYPE XI (OMIM:610968)
OSTEOGENESIS IMPERFECTA, TYPE XIV (OMIM:615066)
Osteogenesis imperfecta type 1 (Orphanet:216796)
Osteogenesis imperfecta type 5 (Orphanet:216828)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 (OMIM:610489)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2 (OMIM:610475)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4 (OMIM:615830)
PMM2-CDG (Orphanet:79318)
Pancreatic insufficiency - anemia - hyperostosis (Orphanet:199337)
Prader-Willi syndrome (Orphanet:739)
Primary pigmented nodular adrenocortical disease (Orphanet:189439)
Proteasome disability syndrome (Orphanet:324977)
Proximal renal tubular acidosis (Orphanet:47159)
Rhizomelic chondrodysplasia punctata type 2 (Orphanet:309796)
SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES (OMIM:615789)
SPONASTRIME dysplasia (Orphanet:93357)
Scheie syndrome (Orphanet:93474)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Senior-Loken syndrome 9 (OMIM:616629)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Spondylo-ocular syndrome (Orphanet:85194)
TENORIO SYNDROME (OMIM:616260)
TRICHORHINOPHALANGEAL SYNDROME, TYPE I (OMIM:190350)
TRICHORHINOPHALANGEAL SYNDROME, TYPE III (OMIM:190351)
Torg-Winchester syndrome (Orphanet:3460)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Urban-Rogers-Meyer syndrome (Orphanet:3409)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)
Werner syndrome (Orphanet:902)
Williams syndrome (Orphanet:904)
Wolcott-Rallison syndrome (Orphanet:1667)
Wrinkly skin syndrome (Orphanet:2834)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)