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病歷用詞 → 對應的 HPO，並附加具這些 HPO 的疾病作為參考。
下肢痠痛
待審核對應 HPO 表現型(2)
- Limb painHP:0009763權重 0.85已確認具此 HPO 的疾病（附加參考）：
- Acute intermittent porphyria (ORPHA:79276)
- Acute peripheral arterial occlusion (ORPHA:90064)
- Classical Ehlers-Danlos syndrome (ORPHA:287)
- Complex regional pain syndrome (ORPHA:83452)
- Encephalitis lethargica (ORPHA:83600)
- Hereditary coproporphyria (ORPHA:79273)
- Hereditary sensory and autonomic neuropathy type 1 (ORPHA:36386)
- Metachromatic leukodystrophy (ORPHA:512)
- Overlap myositis (ORPHA:206572)
- Pantothenate kinase-associated neurodegeneration (ORPHA:157850)
- Spondyloepiphyseal dysplasia tarda (ORPHA:93284)
- Spondylometaphyseal dysplasia, 'corner fracture' type (ORPHA:93315)
- Tick-borne encephalitis (ORPHA:297)
- Von Hippel-Lindau disease (ORPHA:892)
- Bone painHP:0002653權重 0.6已確認具此 HPO 的疾病（附加參考）：
- Acute promyelocytic leukemia (ORPHA:520)
- Adamantinoma (ORPHA:55881)
- Aggressive systemic mastocytosis (ORPHA:98850)
- Albers-Schönberg osteopetrosis (ORPHA:53)
- Aromatase deficiency (ORPHA:91)
- Autosomal dominant hypophosphatemic rickets (ORPHA:89937)
- Autosomal recessive hypophosphatemic rickets (ORPHA:289176)
- Autosomal recessive malignant osteopetrosis (ORPHA:667)
- Blue rubber bleb nevus syndrome (ORPHA:1059)
- Camurati-Engelmann disease (ORPHA:1328)
- Cholestasis-lymphedema syndrome (ORPHA:1414)
- Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis (ORPHA:324964)
- Classic Hodgkin lymphoma (ORPHA:391)
- Congenital alpha2-antiplasmin deficiency (ORPHA:79)
- Cyclic neutropenia (ORPHA:2686)
- Dent disease (ORPHA:1652)
- Dermatitis herpetiformis (ORPHA:1656)
- Distal renal tubular acidosis (ORPHA:18)
- Dysplasia epiphysealis hemimelica (ORPHA:1822)
- Erdheim-Chester disease (ORPHA:35687)
- Familial papillary or follicular thyroid carcinoma (ORPHA:319487)
- Familial tumoral calcinosis (ORPHA:53715)
- Fibrous dysplasia of bone (ORPHA:249)
- Gaucher disease (ORPHA:355)
- Gaucher disease type 1 (ORPHA:77259)
- Gaucher disease type 3 (ORPHA:77261)
- Gorham-Stout disease (ORPHA:73)
- Hajdu-Cheney syndrome (ORPHA:955)
- Hereditary hypophosphatemic rickets with hypercalciuria (ORPHA:157215)
- Hyperparathyroidism-jaw tumor syndrome (ORPHA:99880)
- Hypocalcemic vitamin D-dependent rickets (ORPHA:289157)
- Hypocalcemic vitamin D-resistant rickets (ORPHA:93160)
- Hypophosphatasia (ORPHA:436)
- Idiopathic juvenile osteoporosis (ORPHA:85193)
- Isolated nail clubbing (ORPHA:217059)
- Isolated osteopoikilosis (ORPHA:166119)
- Kienbock disease (ORPHA:97332)
- Langerhans cell histiocytosis (ORPHA:389)
- Maculopapular cutaneous mastocytosis (ORPHA:79457)
- Maffucci syndrome (ORPHA:163634)
- Majeed syndrome (ORPHA:77297)
- Mazabraud syndrome (ORPHA:57782)
- McCune-Albright syndrome (ORPHA:562)
- Melorheostosis (ORPHA:2485)
- Metachondromatosis (ORPHA:2499)
- Mucolipidosis type III alpha/beta (ORPHA:423461)
- Multiple myeloma (ORPHA:29073)
- Myelodysplastic neoplasm with increased blasts (ORPHA:86839)
- Nasu-Hakola disease (ORPHA:2770)
- Neuroblastoma (ORPHA:635)
- Ollier disease (ORPHA:296)
- Oncogenic osteomalacia (ORPHA:352540)
- Osteogenesis imperfecta (ORPHA:666)
- Pachydermoperiostosis (ORPHA:2796)
- Parathyroid carcinoma (ORPHA:143)
- Primary Fanconi renotubular syndrome (ORPHA:3337)
- Primary hyperoxaluria (ORPHA:416)
- Progressive non-infectious anterior vertebral fusion (ORPHA:2062)
- Progressive osseous heteroplasia (ORPHA:2762)
- SAPHO syndrome (ORPHA:793)
- Schnitzler syndrome (ORPHA:37748)
- Secondary non-traumatic avascular necrosis (ORPHA:399180)
- Solitary bone cyst (ORPHA:83468)
- Spastic paraplegia-Paget disease of bone syndrome (ORPHA:329475)
- Spinal arteriovenous metameric syndrome (ORPHA:53721)
- Stickler syndrome (ORPHA:828)
- Systemic mastocytosis with associated hematologic neoplasm (ORPHA:98849)
- Trichorhinophalangeal syndrome type 2 (ORPHA:502)
- Wilson disease (ORPHA:905)
- X-linked hypophosphatemia (ORPHA:89936)