Hypophosphatemia
Symptom Information:
Symptom ID: | HPO:0002148 | ||||||||||||||||||
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) Abnormality of ion homeostasis(HPO:0003111) Abnormality of phosphate homeostasis(HPO:0100529) Hypophosphatemia(HPO:0002148) MedDRA: Investigations(MedDRA:10022891) Water, electrolyte and mineral investigations(MedDRA:10047843) Mineral and electrolyte analyses(MedDRA:10027637) Hypophosphatemia(HPO:0002148) Metabolism and nutrition disorders(MedDRA:10027433) Bone, calcium, magnesium and phosphorus metabolism disorders(MedDRA:10013296) Phosphorus metabolism disorders(MedDRA:10034941) Hypophosphatemia(HPO:0002148) |
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Database Frequency: | 43 / 7739 | ||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Adult hypophosphatasia | (Orphanet:247676) |
Alport syndrome | (Orphanet:63) |
Arterial calcification, generalized, of infancy, 1 | (OMIM:208000) |
Autosomal dominant hypophosphatemic rickets | (Orphanet:89937) |
Autosomal recessive hypophosphatemic rickets | (Orphanet:289176) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Cystinosis | (Orphanet:213) |
Dent disease type 1 | (Orphanet:93622) |
Dent disease type 2 | (Orphanet:93623) |
Dominant hypophosphatemia with nephrolithiasis or osteoporosis | (Orphanet:244305) |
FANCONI RENOTUBULAR SYNDROME 2 | (OMIM:613388) |
Fanconi renotubular syndrome 1 | (OMIM:134600) |
Fatal infantile lactic acidosis with methylmalonic aciduria | (Orphanet:17) |
Glycogen storage disease due to GLUT2 deficiency | (Orphanet:2088) |
HYPOPHOSPHATEMIA, RENAL, WITH INTRACEREBRAL CALCIFICATIONS | (OMIM:241519) |
HYPOPHOSPHATEMIC BONE DISEASE | (OMIM:146350) |
HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM | (OMIM:612089) |
HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE, 1 | (OMIM:241520) |
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE | (OMIM:300554) |
Hereditary fructose intolerance | (Orphanet:469) |
Hereditary hypophosphatemic rickets with hypercalciuria | (Orphanet:157215) |
Hypocalcemic vitamin D-dependent rickets | (Orphanet:289157) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
Hypophosphatemic rickets, autosomal recessive, 2 | (OMIM:613312) |
Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
Linear verrucous nevus syndrome | (Orphanet:2611) |
McCune-Albright syndrome | (Orphanet:562) |
Metaphyseal chondrodysplasia, Jansen type | (Orphanet:33067) |
NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1 | (OMIM:612286) |
NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2 | (OMIM:612287) |
Neonatal severe primary hyperparathyroidism | (Orphanet:417) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Opsismodysplasia | (Orphanet:2746) |
Osteopetrosis | (Orphanet:2781) |
PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS | (OMIM:308990) |
Primary Fanconi syndrome | (Orphanet:3337) |
Proximal renal tubular acidosis | (Orphanet:47159) |
Tyrosinemia type 1 | (Orphanet:882) |
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) |
X-linked hypophosphatemia | (Orphanet:89936) |