Hypophosphatemia

Symptom Information:

Symptom ID: HPO:0002148
Synonyms:
Hypophosphataemia [HPO:0002148]
Hypophosphatemia (disorder) [Orphanet:49300]
Phosphate low [Orphanet:49300]
Hypophosphatemia [Orphanet:49300]
Hypophosphatemia [OMIM:Hypophosphatemia]
Hypophosphataemia [Orphanet:49300]
Blood phosphorus decreased [MedDRA:10049471]
Blood phosphate decreased [MedDRA:10049471]
Phosphate decreased [MedDRA:10049471]
Phosphate low [MedDRA:10049471]
Plasma phosphate decreased [MedDRA:10049471]
Serum inorganic phosphate decreased [MedDRA:10049471]
Serum phosphate decreased [MedDRA:10049471]
Phosphorus low [MedDRA:10049471]
Hypophosphataemia [MedDRA:10021058]
Hypophosphatemia [MedDRA:10021058]
Hypophosphatemia (in some patients) [OMIM:Hypophosphatemia (in some patients)]
Hypophosphatemia (less common) [OMIM:Hypophosphatemia (less common)]
Quality:
Cross references:
Orphanet:49300 "Hypophosphatemia" [Orphanet:49300]
OMIM: "Hypophosphatemia" [OMIM:Hypophosphatemia]
OMIM: "Hypophosphatemia (in some patients)" [OMIM:Hypophosphatemia (in some patients)]
OMIM: "Hypophosphatemia (less common)" [OMIM:Hypophosphatemia (less common)]
UMLS:C0085682 "Hypophosphatemia" [HPO:0002148]
UMLS:C0860987 "Phosphate low" [Orphanet:49300]
UMLS:C0085682 "Hypophosphatemia" [Orphanet:49300]
Is a (Direct Parents):
MedDRA Mineral and electrolyte analyses
MedDRA Phosphorus metabolism disorders
HPO         Abnormality of phosphate homeostasis
Orphanet Abnormality of calcium-phosphate metabolism
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)
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)