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:
Abnormality of lipoprotein cholesterol concentration (HP:0010979)

Parent Node:
Abnormal VLDL cholesterol concentration (HP:0031889)

Parent Node:
Hypolipoproteinemia (HP:0010981)

..Starting node
..Decreased VLDL cholesterol concentration (HP:0031243)

Term ID:

31243

Name:

Decreased VLDL cholesterol concentration

Synonym:

Decreased circulating very-low-density lipoprotein levels

Definition:

A reduction in the amount of very-low-density lipoprotein cholesterol in the blood.

Comments:

Reference:

HP:0031243

Genes and Diseases:

Child Nodes:

Sister Nodes:

Decreased circulating chylomicron concentration (HP:0031242)

Decreased HDL cholesterol concentration (HP:0003233)

Decreased LDL cholesterol concentration (HP:0003563)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031243	HP:0031243	Decreased VLDL cholesterol concentration	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.