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 liver sonography (HP:0031140)

Parent Node:
Abnormal hepatic echogenicity (HP:0031142)

..Starting node
..Decreased hepatic echogenicity (HP:0031143)

Term ID:

31143

Name:

Decreased hepatic echogenicity

Synonym:

Hypoechogenic liver

Definition:

Reduced echogenicity of liver tissue on sonography, manifested as an increased amount of black on the screen of the sonography device.

Comments:

Reference:

HP:0031143

Genes and Diseases:

Child Nodes:

Sister Nodes:

Increased hepatic echogenicity (HP:0031141)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031143	HP:0031143	Decreased hepatic echogenicity	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.