Human Phenotype Ontology

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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

Grandparent Node:
Nephrolithiasis (HP:0000787)

Parent Node:
Calcium nephrolithiasis (HP:0004724)

..Starting node
..Calcium phosphate nephrolithiasis (HP:0012580)

Term ID:

12580

Name:

Calcium phosphate nephrolithiasis

Synonym:

Ca phosphate nephrolithiasis; Ca phosphate urolithiasis; Ca2+ phosphate nephrolitiasis; Ca2+ phosphate urolithiasis; Calcium phosphate urolithiasis

Definition:

The presence of calcium- and phosphate-containing calculi (stones) in the kidneys.

Comments:

Reference:

HP:0012580

Genes and Diseases:

Child Nodes:

Sister Nodes:

Calcium oxalate nephrolithiasis (HP:0008672)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012580	HP:0012580	Calcium phosphate nephrolithiasis	0	CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.