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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。
Elevated circulating alkaline phosphatase concentration
HP:0003155
對應病歷用詞(1)
- high alkaline phosphatase權重 0.8待審核
具此 HPO 的疾病（附加參考）(42)
- Spastic paraplegia-Paget disease of bone syndromeORPHA:329475 · Obligate (100%)
- Hyperphosphatasia-intellectual disability syndromeORPHA:247262 · Very frequent (99-80%)
- Lysosomal acid lipase deficiencyORPHA:275761 · Very frequent (99-80%)
- Neonatal intrahepatic cholestasis due to citrin deficiencyORPHA:247598 · Very frequent (99-80%)
- Oncogenic osteomalaciaORPHA:352540 · Very frequent (99-80%)
- X-linked hypophosphatemiaORPHA:89936 · Very frequent (99-80%)
- Adult-onset Still diseaseORPHA:829 · Frequent (79-30%)
- Aggressive systemic mastocytosisORPHA:98850 · Frequent (79-30%)
- Autosomal dominant hypophosphatemic ricketsORPHA:89937 · Frequent (79-30%)
- Budd-Chiari syndromeORPHA:131 · Frequent (79-30%)
- Caroli diseaseORPHA:53035 · Frequent (79-30%)
- Caroli syndromeORPHA:480520 · Frequent (79-30%)
- COG4-CDGORPHA:263501 · Frequent (79-30%)
- Congenital bile acid synthesis defect type 2ORPHA:79303 · Frequent (79-30%)
- Congenital bile acid synthesis defect type 3ORPHA:79302 · Frequent (79-30%)
- Congenital hyperinsulinism due to HNF4A deficiencyORPHA:263455 · Frequent (79-30%)
- CystinosisORPHA:213 · Frequent (79-30%)
- Enamel-renal syndromeORPHA:1031 · Frequent (79-30%)
- Fibrous dysplasia of boneORPHA:249 · Frequent (79-30%)
- Hypocalcemic vitamin D-dependent ricketsORPHA:289157 · Frequent (79-30%)
- Inclusion body myopathy with Paget disease of bone and frontotemporal dementiaORPHA:52430 · Frequent (79-30%)
- Isolated biliary atresiaORPHA:30391 · Frequent (79-30%)
- Metaphyseal chondrodysplasia, Jansen typeORPHA:33067 · Frequent (79-30%)
- Mirizzi syndromeORPHA:521219 · Frequent (79-30%)
- OsteosarcomaORPHA:668 · Frequent (79-30%)
- Parenteral nutrition-associated cholestasisORPHA:567983 · Frequent (79-30%)
- Primary biliary cholangitisORPHA:186 · Frequent (79-30%)
- Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestationsORPHA:247691 · Frequent (79-30%)
- Senior-Boichis syndromeORPHA:84081 · Frequent (79-30%)
- TAFRO syndromeORPHA:457077 · Frequent (79-30%)
- Wild type ATTR amyloidosisORPHA:330001 · Frequent (79-30%)
- AL amyloidosisORPHA:85443 · Occasional (29-5%)
- Cystic echinococcosisORPHA:400 · Occasional (29-5%)
- Fanconi-Bickel syndromeORPHA:2088 · Occasional (29-5%)
- Graft versus host diseaseORPHA:39812 · Occasional (29-5%)
- Intermediate osteopetrosisORPHA:210110 · Occasional (29-5%)
- Intrahepatic cholestasis of pregnancyORPHA:69665 · Occasional (29-5%)
- Isolated polycystic liver diseaseORPHA:2924 · Occasional (29-5%)
- Neuroleptic malignant syndromeORPHA:94093 · Occasional (29-5%)
- Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndromeORPHA:562639 · Occasional (29-5%)
- Amoebiasis due to Entamoeba histolyticaORPHA:67 · Very rare (<4-1%)
- Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndromeORPHA:529665 · Excluded (0%)