Human Phenotype Ontology

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

Grandparent Node:
Abnormal circulating protein concentration (HP:0010876)

Parent Node:
Abnormal circulating albumin concentration (HP:0012116)

..Starting node
..Hyperalbuminemia (HP:0012117)

Term ID:

12117

Name:

Hyperalbuminemia

Synonym:

High albumin; High blood albumin levels; Hyperalbuminaemia

Definition:

Elevation in the concentration of albumin in the blood.

Comments:

Reference:

HP:0012117

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hypoalbuminemia (HP:0003073)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012117	HP:0012117	Hyperalbuminemia	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.