Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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: Bone Demineralization, Pathologic (D018488)
Parent Node: Calcium Metabolism Disorders (D002128)
..Starting node ..Decalcification, Pathologic (D003649)
Child Nodes:
........Van Bogaert-Hozay syndrome (C536526)
Sister Nodes:
..Calcinosis (D002114) 50
..Decalcification, Pathologic (D003649) 1
..Hypercalcemia (D006934) 10
..Hypocalcemia (D006996) 5
..Hypouricemia, Hypercalcinuria, and Decreased Bone Density (C565475)
..Meier Blumberg Imahorn syndrome (C536148)
..Pseudohypoparathyroidism (D011547) 6
..Rickets (D012279) 16
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	3141
Name:	Decalcification, Pathologic
Definition:	The loss of calcium salts from bones and teeth. Bacteria may be responsible for this occurrence in teeth. Old age may be a factor contributing to calcium loss, as is the presence of diseases such as rheumatoid arthritis.
Alternative IDs:
ParentIDs:	MESH:D002128\|MESH:D018488
TreeNumbers:	C05.116.198.247.400 \|C18.452.174.289
Synonyms:	Decalcification, Pathological \|Pathological Decalcification \|Pathologic Decalcification
Slim Mappings:	Metabolic disease\|Musculoskeletal disease
Reference:	MedGen: D003649 MeSH: D003649 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants