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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Metabolic Diseases (D008659)
..Starting node ..Phosphorus Metabolism Disorders (D010760)
Child Nodes:
........Hyperphosphatasia with Mental Retardation (C565495) 2
........Hyperphosphatemia (D054559) 3
........Hypophosphatemia (D017674) 17
Sister Nodes:
..Acid-Base Imbalance (D000137) 42
..ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 2 (OMIM:606770)
..ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 3 (OMIM:606771)
..Brain Diseases, Metabolic (D001928) 244
..Calcium Metabolism Disorders (D002128) 94
..DNA Repair-Deficiency Disorders (D049914) 95
..Glucose Metabolism Disorders (D044882) 137
..Hyperlactatemia (D065906)
..Hypermanganesemia with Dystonia Polycythemia and Cirrhosis (C548016)
..Iron Metabolism Disorders (D019189) 23
..Lipid Metabolism Disorders (D052439) 189
..Malabsorption Syndromes (D008286) 29
..Metabolic Syndrome X (D024821) 1
..Metabolism, Inborn Errors (D008661) 886
..Mitochondrial Diseases (D028361) 114
..Phosphorus Metabolism Disorders (D010760) 25
..Porphyrias (D011164) 18
..Proteostasis Deficiencies (D057165) 55
..SHORT syndrome (C537327)
..Skin Diseases, Metabolic (D012875) 33
..Wasting Syndrome (D019282) 1
..Water-Electrolyte Imbalance (D014883) 31
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8910
Name:	Phosphorus Metabolism Disorders
Definition:	Disorders in the processing of phosphorus in the body: its absorption, transport, storage, and utilization.
Alternative IDs:
ParentIDs:	MESH:D008659
TreeNumbers:	C18.452.750
Synonyms:	Disorder, Phosphorus Metabolism \|Disorders, Phosphorus Metabolism \|Metabolism Disorder, Phosphorus \|Metabolism Disorders, Phosphorus \|Phosphorus Metabolism Disorder
Slim Mappings:	Metabolic disease
Reference:	MedGen: D010760 MeSH: D010760 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants