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 circulating thyroid hormone concentration (HP:0031508)

Parent Node:
Abnormal T3/T4 ratio (HP:0012558)

..Starting node
..Decreased T3/T4 ratio (HP:0012560)

Term ID:

12560

Name:

Decreased T3/T4 ratio

Synonym:

Definition:

A ratio of serum triiodothyronine (T3) to thyroxine (T4) in the blood that is lower than normal.

Comments:

Reference:

HP:0012560

Genes and Diseases:

Child Nodes:

Sister Nodes:

Increased T3/T4 ratio (HP:0012559)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012560	HP:0012560	Decreased T3/T4 ratio	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.