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HPO → 對應的病歷用詞，並附加具此 HPO 的疾病作為參考。
Reduced bone mineral density
HP:0004349
對應病歷用詞(0)
尚無對應用詞。
具此 HPO 的疾病（附加參考）(76)
- 46,XY difference of sex development due to isolated 17,20-lyase deficiencyORPHA:90796 · Very frequent (99-80%)
- 46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiencyORPHA:168558 · Very frequent (99-80%)
- Atypical Werner syndromeORPHA:79474 · Very frequent (99-80%)
- Autosomal recessive malignant osteopetrosisORPHA:667 · Very frequent (99-80%)
- Coxoauricular syndromeORPHA:1508 · Very frequent (99-80%)
- Difference of sex development-intellectual disability syndromeORPHA:2983 · Very frequent (99-80%)
- Distal renal tubular acidosisORPHA:18 · Very frequent (99-80%)
- Hallermann-Streiff syndromeORPHA:2108 · Very frequent (99-80%)
- Hereditary sensory and autonomic neuropathy type 2ORPHA:970 · Very frequent (99-80%)
- Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiencyORPHA:289548 · Very frequent (99-80%)
- Intellectual disability, Buenos-Aires typeORPHA:3079 · Very frequent (99-80%)
- Larsen-like osseous dysplasia-short stature syndromeORPHA:2370 · Very frequent (99-80%)
- Metaphyseal chondrodysplasia, Spahr typeORPHA:2501 · Very frequent (99-80%)
- Microcephalic primordial dwarfism, Montreal typeORPHA:2617 · Very frequent (99-80%)
- Mucopolysaccharidosis type 4ORPHA:582 · Very frequent (99-80%)
- Nasu-Hakola diseaseORPHA:2770 · Very frequent (99-80%)
- Phakomatosis pigmentovascularisORPHA:2875 · Very frequent (99-80%)
- Seizures-scoliosis-macrocephaly syndromeORPHA:466926 · Very frequent (99-80%)
- Spinocerebellar ataxia-dysmorphism syndromeORPHA:1185 · Very frequent (99-80%)
- X small rings syndromeORPHA:96201 · Very frequent (99-80%)
- Xp21 deletion syndromeORPHA:261476 · Very frequent (99-80%)
- 46,XX gonadal dysgenesisORPHA:243 · Frequent (79-30%)
- AdrenomyodystrophyORPHA:977 · Frequent (79-30%)
- Beta-thalassemiaORPHA:848 · Frequent (79-30%)
- Beta-thalassemia intermediaORPHA:231222 · Frequent (79-30%)
- Cooper-Jabs syndromeORPHA:1488 · Frequent (79-30%)
- Free sialic acid storage diseaseORPHA:834 · Frequent (79-30%)
- Hereditary hypophosphatemic rickets with hypercalciuriaORPHA:157215 · Frequent (79-30%)
- Hypergonadotropic hypogonadism-cataract syndromeORPHA:2410 · Frequent (79-30%)
- Hypogonadotropic hypogonadism-retinitis pigmentosa syndromeORPHA:2235 · Frequent (79-30%)
- Kallmann syndromeORPHA:478 · Frequent (79-30%)
- Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndromeORPHA:83629 · Frequent (79-30%)
- Lipodystrophy due to peptidic growth factors deficiencyORPHA:1979 · Frequent (79-30%)
- Marshall-Smith syndromeORPHA:561 · Frequent (79-30%)
- Multiple endocrine neoplasia type 1ORPHA:652 · Frequent (79-30%)
- Orofaciodigital syndrome type 1ORPHA:2750 · Frequent (79-30%)
- Osteogenesis imperfectaORPHA:666 · Frequent (79-30%)
- Progressive familial intrahepatic cholestasisORPHA:172 · Frequent (79-30%)
- Rothmund-Thomson syndromeORPHA:2909 · Frequent (79-30%)
- Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndromeORPHA:137608 · Frequent (79-30%)
- Short-limb skeletal dysplasia with severe combined immunodeficiencyORPHA:935 · Frequent (79-30%)
- X-linked hypophosphatemiaORPHA:89936 · Frequent (79-30%)
- Alacrimia-choreoathetosis-liver dysfunction syndromeORPHA:404454 · Occasional (29-5%)
- AlkaptonuriaORPHA:56 · Occasional (29-5%)
- Autosomal dominant hypocalcemiaORPHA:428 · Occasional (29-5%)
- Cholestasis-lymphedema syndromeORPHA:1414 · Occasional (29-5%)
- CINCA syndromeORPHA:1451 · Occasional (29-5%)
- Classic galactosemiaORPHA:79239 · Occasional (29-5%)
- Cutis marmorata telangiectatica congenitaORPHA:1556 · Occasional (29-5%)
- Fabry diseaseORPHA:324 · Occasional (29-5%)
- Familial calcium pyrophosphate depositionORPHA:1416 · Occasional (29-5%)
- Familial exudative vitreoretinopathyORPHA:891 · Occasional (29-5%)
- Fanconi anemiaORPHA:84 · Occasional (29-5%)
- Friedreich ataxiaORPHA:95 · Occasional (29-5%)
- Hutchinson-Gilford progeria syndromeORPHA:740 · Occasional (29-5%)
- Linear verrucous nevus syndromeORPHA:2611 · Occasional (29-5%)
- Marfan syndromeORPHA:558 · Occasional (29-5%)
- Monosomy X syndromeORPHA:99226 · Occasional (29-5%)
- Mosaic monosomy X syndromeORPHA:99228 · Occasional (29-5%)
- Mucolipidosis type IIIORPHA:577 · Occasional (29-5%)
- Mucopolysaccharidosis type 3ORPHA:581 · Occasional (29-5%)
- Nail-patella syndromeORPHA:2614 · Occasional (29-5%)
- Oculocerebral hypopigmentation syndrome, Preus typeORPHA:2720 · Occasional (29-5%)
- Poland syndromeORPHA:2911 · Occasional (29-5%)
- Prolidase deficiencyORPHA:742 · Occasional (29-5%)
- Proximal renal tubular acidosisORPHA:47159 · Occasional (29-5%)
- Pseudohypoparathyroidism type 1AORPHA:79443 · Occasional (29-5%)
- Rheumatoid factor-positive polyarticular juvenile idiopathic arthritisORPHA:85435 · Occasional (29-5%)
- Richards-Rundle syndromeORPHA:1399 · Occasional (29-5%)
- Short stature due to primary acid-labile subunit deficiencyORPHA:140941 · Occasional (29-5%)
- Spondyloepiphyseal dysplasia congenitaORPHA:94068 · Occasional (29-5%)
- Stickler syndromeORPHA:828 · Occasional (29-5%)
- Trisomy 20p syndromeORPHA:261318 · Occasional (29-5%)
- Turner syndromeORPHA:881 · Occasional (29-5%)
- Turner syndrome due to structural X chromosome anomaliesORPHA:99413 · Occasional (29-5%)
- Spondylometaphyseal dysplasia, 'corner fracture' typeORPHA:93315 · Very rare (<4-1%)