Elevated alkaline phosphatase
Symptom Information:
Symptom ID: | HPO:0003155 | ||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormal enzyme/coenzyme activity(HPO:0012379) Abnormality of alkaline phosphatase activity(HPO:0004379) Elevated alkaline phosphatase(HPO:0003155) MedDRA: |
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Database Frequency: | 52 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
ALKALINE PHOSPHATASE, PLASMA LEVEL OF, QUANTITATIVE TRAIT LOCUS 1 | (OMIM:171720) |
AMYOTROPHIC LATERAL SCLEROSIS 20 | (OMIM:615426) |
ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS | (OMIM:108050) |
Alström syndrome | (Orphanet:64) |
Autosomal dominant hypophosphatemic rickets | (Orphanet:89937) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
Benign recurrent intrahepatic cholestasis type 2 | (Orphanet:99961) |
COG4-CDG | (Orphanet:263501) |
CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT | (OMIM:122860) |
CRANIOMETADIAPHYSEAL DYSPLASIA | (OMIM:269300) |
Calvarial doughnut lesions - bone fragility | (Orphanet:85192) |
Cholestasis - lymphedema | (Orphanet:1414) |
Congenital bile acid synthesis defect type 2 | (Orphanet:79303) |
Congenital bile acid synthesis defect type 3 | (Orphanet:79302) |
Craniodiaphyseal dysplasia | (Orphanet:1513) |
Craniometadiaphyseal dysplasia, wormian bone type | (Orphanet:85184) |
Familial expansile osteolysis | (Orphanet:85195) |
Glycogen storage disease due to GLUT2 deficiency | (Orphanet:2088) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 | (OMIM:239300) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2 | (OMIM:614749) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3 | (OMIM:614207) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4 | (OMIM:615716) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 5 | (OMIM:616025) |
Hereditary hypophosphatemic rickets with hypercalciuria | (Orphanet:157215) |
Hyperostosis corticalis generalisata | (Orphanet:3416) |
Hyperphosphatasia-intellectual deficiency syndrome | (Orphanet:247262) |
Hypocalcemic vitamin D-dependent rickets | (Orphanet:289157) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
Hypophosphatemic rickets, autosomal recessive, 2 | (OMIM:613312) |
Isolated polycystic liver disease | (Orphanet:2924) |
Lathosterolosis | (Orphanet:46059) |
Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
Low phospholipid associated cholelithiasis | (Orphanet:69663) |
Metaphyseal chondrodysplasia, Jansen type | (Orphanet:33067) |
Morgagni-Stewart-Morel syndrome | (Orphanet:77296) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
OSTEOGENESIS IMPERFECTA, TYPE XI | (OMIM:610968) |
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1 | (OMIM:259700) |
OSTEOSCLEROTIC METAPHYSEAL DYSPLASIA | (OMIM:615198) |
PAGET DISEASE OF BONE | (OMIM:602080) |
PAGET DISEASE OF BONE 1 | (OMIM:167250) |
PAGET DISEASE OF BONE 4 | (OMIM:606263) |
Pearson syndrome | (Orphanet:699) |
Primary Fanconi syndrome | (Orphanet:3337) |
Progressive familial intrahepatic cholestasis type 2 | (Orphanet:79304) |
Reynolds syndrome | (Orphanet:779) |
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A | (OMIM:264700) |
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B | (OMIM:600081) |
VITAMIN D-DEPENDENT RICKETS, TYPE 2A | (OMIM:277440) |
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR | (OMIM:600785) |
X-linked hypophosphatemia | (Orphanet:89936) |