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:
Abnormal renal morphology (HP:0012210)

Parent Node:
Nephrocalcinosis (HP:0000121)

..Starting node
..Microscopic nephrocalcinosis (HP:0008327)

Term ID:

8327

Name:

Microscopic nephrocalcinosis

Synonym:

Definition:

The presence of microscopic crystalline calcium precipitates in the form of oxalate and/or phosphate in the renal parenchyma.

Comments:

Reference:

HP:0008327

Genes and Diseases:

Child Nodes:

Sister Nodes:

Cortical nephrocalcinosis (HP:0012409)

Medullary nephrocalcinosis (HP:0012408)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008327	HP:0008327	Microscopic nephrocalcinosis	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.