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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。
high alkaline phosphatase
待審核對應 HPO 表現型(1)
- 權重 0.8待審核具此 HPO 的疾病（附加參考）：
- Adult-onset Still disease (ORPHA:829)
- Aggressive systemic mastocytosis (ORPHA:98850)
- AL amyloidosis (ORPHA:85443)
- Amoebiasis due to Entamoeba histolytica (ORPHA:67)
- Autosomal dominant hypophosphatemic rickets (ORPHA:89937)
- Budd-Chiari syndrome (ORPHA:131)
- Caroli disease (ORPHA:53035)
- Caroli syndrome (ORPHA:480520)
- COG4-CDG (ORPHA:263501)
- Congenital bile acid synthesis defect type 2 (ORPHA:79303)
- Congenital bile acid synthesis defect type 3 (ORPHA:79302)
- Congenital hyperinsulinism due to HNF4A deficiency (ORPHA:263455)
- Cystic echinococcosis (ORPHA:400)
- Cystinosis (ORPHA:213)
- Enamel-renal syndrome (ORPHA:1031)
- Fanconi-Bickel syndrome (ORPHA:2088)
- Fibrous dysplasia of bone (ORPHA:249)
- Graft versus host disease (ORPHA:39812)
- Hyperphosphatasia-intellectual disability syndrome (ORPHA:247262)
- Hypocalcemic vitamin D-dependent rickets (ORPHA:289157)
- Inclusion body myopathy with Paget disease of bone and frontotemporal dementia (ORPHA:52430)
- Intermediate osteopetrosis (ORPHA:210110)
- Intrahepatic cholestasis of pregnancy (ORPHA:69665)
- Isolated biliary atresia (ORPHA:30391)
- Isolated polycystic liver disease (ORPHA:2924)
- Lysosomal acid lipase deficiency (ORPHA:275761)
- Metaphyseal chondrodysplasia, Jansen type (ORPHA:33067)
- Mirizzi syndrome (ORPHA:521219)
- Neonatal intrahepatic cholestasis due to citrin deficiency (ORPHA:247598)
- Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome (ORPHA:529665)
- Neuroleptic malignant syndrome (ORPHA:94093)
- Oncogenic osteomalacia (ORPHA:352540)
- Osteosarcoma (ORPHA:668)
- Parenteral nutrition-associated cholestasis (ORPHA:567983)
- Primary biliary cholangitis (ORPHA:186)
- Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome (ORPHA:562639)
- Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations (ORPHA:247691)
- Senior-Boichis syndrome (ORPHA:84081)
- Spastic paraplegia-Paget disease of bone syndrome (ORPHA:329475)
- TAFRO syndrome (ORPHA:457077)
- Wild type ATTR amyloidosis (ORPHA:330001)
- X-linked hypophosphatemia (ORPHA:89936)