Reduced bone mineral density
Symptom Information:
Symptom ID: | HPO:0004349 | ||
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) MedDRA: |
||
Database Frequency: | 165 / 7739 | ||
Resource: |
All diseases associated with this symptom:
46,XX gonadal dysgenesis | (Orphanet:243) |
ACTH-dependent Cushing syndrome | (Orphanet:99892) |
ACTH-independent macronodular adrenal hyperplasia | (Orphanet:189427) |
Acroosteolysis, dominant type | (Orphanet:955) |
Adrenomyodystrophy | (Orphanet:977) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Alexander disease | (Orphanet:58) |
Alkaptonuria | (Orphanet:56) |
Amish lethal microcephaly | (Orphanet:99742) |
Aromatase deficiency | (Orphanet:91) |
Atypical Rett syndrome | (Orphanet:3095) |
Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
Autosomal dominant hypocalcemia | (Orphanet:428) |
Autosomal dominant hypophosphatemic rickets | (Orphanet:89937) |
Autosomal recessive cutis laxa type 1 | (Orphanet:90349) |
Autosomal recessive cutis laxa type 2 | (Orphanet:90350) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
Beta-thalassemia | (Orphanet:848) |
Beta-thalassemia major | (Orphanet:231214) |
Bird headed-dwarfism, Montreal type | (Orphanet:2617) |
Brittle cornea syndrome | (Orphanet:90354) |
Bruck syndrome | (Orphanet:2771) |
CARDIOFACIOCUTANEOUS SYNDROME 3 | (OMIM:615279) |
CINCA syndrome | (Orphanet:1451) |
Carney complex | (Orphanet:1359) |
Cholestasis - lymphedema | (Orphanet:1414) |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | (Orphanet:90794) |
Classic galactosemia | (Orphanet:79239) |
Classical homocystinuria | (Orphanet:394) |
Cleidocranial dysplasia | (Orphanet:1452) |
Cole-Carpenter syndrome | (Orphanet:2050) |
Complete androgen insensitivity syndrome | (Orphanet:99429) |
Congenital bile acid synthesis defect type 1 | (Orphanet:79301) |
Congenital bile acid synthesis defect type 2 | (Orphanet:79303) |
Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
Congenital erythropoietic porphyria | (Orphanet:79277) |
Cooper-Jabs syndrome | (Orphanet:1488) |
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis | (Orphanet:94062) |
Coxoauricular syndrome | (Orphanet:1508) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Cushing syndrome due to ectopic ACTH secretion | (Orphanet:99889) |
Cutaneous mastocytosis | (Orphanet:66646) |
Cutis marmorata telangiectatica congenita | (Orphanet:1556) |
Cyprus facial-neuromusculoskeletal syndrome | (Orphanet:2674) |
Cystinosis | (Orphanet:213) |
De Barsy syndrome | (Orphanet:2962) |
Dent disease type 1 | (Orphanet:93622) |
Disorder of bile acid synthesis | (Orphanet:79168) |
Disorder of sex development - intellectual deficit | (Orphanet:2983) |
Duchenne and Becker muscular dystrophy | (Orphanet:262) |
Dyskeratosis congenita | (Orphanet:1775) |
Ehlers-Danlos syndrome type 7B | (Orphanet:99876) |
Ehlers-Danlos syndrome, dermatosparaxis type | (Orphanet:1901) |
Ehlers-Danlos syndrome, progeroid type | (Orphanet:75496) |
Ehlers-Danlos syndrome, spondylocheirodysplastic type | (Orphanet:157965) |
Extensor tendons of finger anomalies | (Orphanet:3294) |
FANCONI RENOTUBULAR SYNDROME 2 | (OMIM:613388) |
Fabry disease | (Orphanet:324) |
Fanconi anemia | (Orphanet:84) |
Farber lipogranulomatosis | (Orphanet:333) |
Free sialic acid storage disease | (Orphanet:834) |
Galactosemia | (Orphanet:352) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 1 | (Orphanet:77259) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Geroderma osteodysplastica | (Orphanet:2078) |
Gnathodiaphyseal dysplasia | (Orphanet:53697) |
Grange syndrome | (Orphanet:79094) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hemochromatosis type 2 | (Orphanet:79230) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hereditary hypophosphatemic rickets with hypercalciuria | (Orphanet:157215) |
Hereditary sensory and autonomic neuropathy type 2 | (Orphanet:970) |
Hutchinson-Gilford progeria syndrome | (Orphanet:740) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
Idiopathic juvenile osteoporosis | (Orphanet:85193) |
Indolent systemic mastocytosis | (Orphanet:98848) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy | (Orphanet:2958) |
Isolated glycerol kinase deficiency | (Orphanet:408) |
Juvenile Paget disease | (Orphanet:2801) |
Kaler-Garrity-Stern syndrome | (Orphanet:2324) |
Kallmann syndrome | (Orphanet:478) |
Larsen-like osseous dysplasia - short stature | (Orphanet:2370) |
Lichstenstein syndrome | (Orphanet:2390) |
Linear verrucous nevus syndrome | (Orphanet:2611) |
Lipodystrophy due to peptidic growth factors deficiency | (Orphanet:1979) |
Lowry-MacLean syndrome | (Orphanet:2409) |
Marfan syndrome | (Orphanet:558) |
Marshall-Smith syndrome | (Orphanet:561) |
Mastocytosis | (Orphanet:98292) |
McCune-Albright syndrome | (Orphanet:562) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
Menkes disease | (Orphanet:565) |
Metaphyseal chondrodysplasia, Spahr type | (Orphanet:2501) |
Metaphyseal dysplasia - maxillary hypoplasia - brachydacty | (Orphanet:2504) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Mikati-Najjar-Sahli syndrome | (Orphanet:2558) |
Mu heavy-chain disease | (Orphanet:100024) |
Mucolipidosis type 3 | (Orphanet:577) |
Mucopolysaccharidosis type 4 | (Orphanet:582) |
Nasu-Hakola disease | (Orphanet:2770) |
Neu-Laxova syndrome | (Orphanet:2671) |
OSTEOGENESIS IMPERFECTA, TYPE XI | (OMIM:610968) |
Occipital horn syndrome | (Orphanet:198) |
Oculocerebral hypopigmentation syndrome, Preus type | (Orphanet:2720) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Oculocutaneous albinism type 1A | (Orphanet:79431) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Osteochondrodysplatic nanism - deafness - retinitis pigmentosa | (Orphanet:2653) |
Osteogenesis imperfecta | (Orphanet:666) |
Osteogenesis imperfecta type 4 | (Orphanet:216820) |
Osteopenia - myopia - hearing loss - intellectual deficit - facial dysmorphism | (Orphanet:91133) |
Osteopetrosis | (Orphanet:2781) |
Osteopetrosis with renal tubular acidosis | (Orphanet:2785) |
Osteoporosis - macrocephaly - blindness - joint hyperlaxity | (Orphanet:2787) |
Osteoporosis - pseudoglioma | (Orphanet:2788) |
Pachydermoperiostosis | (Orphanet:2796) |
Parastremmatic dwarfism | (Orphanet:2646) |
Partial androgen insensitivity syndrome | (Orphanet:90797) |
Pearson syndrome | (Orphanet:699) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Phakomatosis pigmentovascularis | (Orphanet:2875) |
Poland syndrome | (Orphanet:2911) |
Primary hyperoxaluria | (Orphanet:416) |
Primary intestinal lymphangiectasia | (Orphanet:90362) |
Primary pigmented nodular adrenocortical disease | (Orphanet:189439) |
Progressive familial intrahepatic cholestasis | (Orphanet:172) |
Prolidase deficiency | (Orphanet:742) |
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia | (Orphanet:3390) |
Pseudoprogeria syndrome | (Orphanet:2985) |
Recessive dystrophic epidermolysis bullosa-generalized other | (Orphanet:89842) |
Rett syndrome | (Orphanet:778) |
Richards-Rundle syndrome | (Orphanet:1399) |
Richieri Costa-da Silva syndrome | (Orphanet:3101) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Rothmund-Thomson syndrome type 2 | (Orphanet:221016) |
SPONASTRIME dysplasia | (Orphanet:93357) |
Sakati-Nyhan syndrome | (Orphanet:3128) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus | (Orphanet:137608) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
Short-limb skeletal dysplasia with severe combined immunodeficiency | (Orphanet:935) |
Shprintzen-Goldberg syndrome | (Orphanet:2462) |
Shwachman-Diamond syndrome | (Orphanet:811) |
Sialidosis type 2 | (Orphanet:87876) |
Spinocerebellar ataxia - dysmorphism | (Orphanet:1185) |
Spondylo-ocular syndrome | (Orphanet:85194) |
Spondyloepimetaphyseal dysplasia, Irapa type | (Orphanet:93351) |
Stickler syndrome | (Orphanet:828) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
Systemic mastocytosis | (Orphanet:2467) |
Telecanthus - hypertelorism - strabismus - pes cavus | (Orphanet:3293) |
Torg-Winchester syndrome | (Orphanet:3460) |
Trisomy 20p | (Orphanet:261318) |
Turner syndrome | (Orphanet:881) |
Urban-Rogers-Meyer syndrome | (Orphanet:3409) |
Werner syndrome | (Orphanet:902) |
Williams syndrome | (Orphanet:904) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
X-linked hypophosphatemia | (Orphanet:89936) |