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以 HPO 交叉檢視
HPO → 對應的病歷用詞,並附加具此 HPO 的疾病作為參考。
Bone pain
HP:0002653
對應病歷用詞(3)
具此 HPO 的疾病(附加參考)(70)
- Albers-Schönberg osteopetrosisORPHA:53 · Very frequent (99-80%)
- Aromatase deficiencyORPHA:91 · Very frequent (99-80%)
- Autosomal recessive hypophosphatemic ricketsORPHA:289176 · Very frequent (99-80%)
- Autosomal recessive malignant osteopetrosisORPHA:667 · Very frequent (99-80%)
- Blue rubber bleb nevus syndromeORPHA:1059 · Very frequent (99-80%)
- Camurati-Engelmann diseaseORPHA:1328 · Very frequent (99-80%)
- Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitisORPHA:324964 · Very frequent (99-80%)
- Cyclic neutropeniaORPHA:2686 · Very frequent (99-80%)
- Dysplasia epiphysealis hemimelicaORPHA:1822 · Very frequent (99-80%)
- Erdheim-Chester diseaseORPHA:35687 · Very frequent (99-80%)
- Familial tumoral calcinosisORPHA:53715 · Very frequent (99-80%)
- Gaucher disease type 1ORPHA:77259 · Very frequent (99-80%)
- Hypocalcemic vitamin D-dependent ricketsORPHA:289157 · Very frequent (99-80%)
- Hypocalcemic vitamin D-resistant ricketsORPHA:93160 · Very frequent (99-80%)
- Idiopathic juvenile osteoporosisORPHA:85193 · Very frequent (99-80%)
- Kienbock diseaseORPHA:97332 · Very frequent (99-80%)
- Langerhans cell histiocytosisORPHA:389 · Very frequent (99-80%)
- Majeed syndromeORPHA:77297 · Very frequent (99-80%)
- MelorheostosisORPHA:2485 · Very frequent (99-80%)
- MetachondromatosisORPHA:2499 · Very frequent (99-80%)
- Nasu-Hakola diseaseORPHA:2770 · Very frequent (99-80%)
- PachydermoperiostosisORPHA:2796 · Very frequent (99-80%)
- Progressive osseous heteroplasiaORPHA:2762 · Very frequent (99-80%)
- SAPHO syndromeORPHA:793 · Very frequent (99-80%)
- Schnitzler syndromeORPHA:37748 · Very frequent (99-80%)
- Spastic paraplegia-Paget disease of bone syndromeORPHA:329475 · Very frequent (99-80%)
- Spinal arteriovenous metameric syndromeORPHA:53721 · Very frequent (99-80%)
- Trichorhinophalangeal syndrome type 2ORPHA:502 · Very frequent (99-80%)
- Wilson diseaseORPHA:905 · Very frequent (99-80%)
- AdamantinomaORPHA:55881 · Frequent (79-30%)
- Aggressive systemic mastocytosisORPHA:98850 · Frequent (79-30%)
- Autosomal dominant hypophosphatemic ricketsORPHA:89937 · Frequent (79-30%)
- Dent diseaseORPHA:1652 · Frequent (79-30%)
- Fibrous dysplasia of boneORPHA:249 · Frequent (79-30%)
- Gaucher diseaseORPHA:355 · Frequent (79-30%)
- Gaucher disease type 3ORPHA:77261 · Frequent (79-30%)
- Gorham-Stout diseaseORPHA:73 · Frequent (79-30%)
- Hajdu-Cheney syndromeORPHA:955 · Frequent (79-30%)
- Hereditary hypophosphatemic rickets with hypercalciuriaORPHA:157215 · Frequent (79-30%)
- HypophosphatasiaORPHA:436 · Frequent (79-30%)
- Maffucci syndromeORPHA:163634 · Frequent (79-30%)
- Mucolipidosis type III alpha/betaORPHA:423461 · Frequent (79-30%)
- Multiple myelomaORPHA:29073 · Frequent (79-30%)
- Ollier diseaseORPHA:296 · Frequent (79-30%)
- Oncogenic osteomalaciaORPHA:352540 · Frequent (79-30%)
- Osteogenesis imperfectaORPHA:666 · Frequent (79-30%)
- Primary Fanconi renotubular syndromeORPHA:3337 · Frequent (79-30%)
- Primary hyperoxaluriaORPHA:416 · Frequent (79-30%)
- Secondary non-traumatic avascular necrosisORPHA:399180 · Frequent (79-30%)
- Solitary bone cystORPHA:83468 · Frequent (79-30%)
- Stickler syndromeORPHA:828 · Frequent (79-30%)
- X-linked hypophosphatemiaORPHA:89936 · Frequent (79-30%)
- Acute promyelocytic leukemiaORPHA:520 · Occasional (29-5%)
- Cholestasis-lymphedema syndromeORPHA:1414 · Occasional (29-5%)
- Classic Hodgkin lymphomaORPHA:391 · Occasional (29-5%)
- Congenital alpha2-antiplasmin deficiencyORPHA:79 · Occasional (29-5%)
- Dermatitis herpetiformisORPHA:1656 · Occasional (29-5%)
- Distal renal tubular acidosisORPHA:18 · Occasional (29-5%)
- Familial papillary or follicular thyroid carcinomaORPHA:319487 · Occasional (29-5%)
- Hyperparathyroidism-jaw tumor syndromeORPHA:99880 · Occasional (29-5%)
- Isolated osteopoikilosisORPHA:166119 · Occasional (29-5%)
- Maculopapular cutaneous mastocytosisORPHA:79457 · Occasional (29-5%)
- Mazabraud syndromeORPHA:57782 · Occasional (29-5%)
- McCune-Albright syndromeORPHA:562 · Occasional (29-5%)
- Myelodysplastic neoplasm with increased blastsORPHA:86839 · Occasional (29-5%)
- NeuroblastomaORPHA:635 · Occasional (29-5%)
- Parathyroid carcinomaORPHA:143 · Occasional (29-5%)
- Progressive non-infectious anterior vertebral fusionORPHA:2062 · Occasional (29-5%)
- Systemic mastocytosis with associated hematologic neoplasmORPHA:98849 · Occasional (29-5%)
- Isolated nail clubbingORPHA:217059 · Excluded (0%)