Osteopenia
Symptom Information:
Symptom ID: | HPO:0000938 | ||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |