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:
Acidosis (HP:0001941)

Parent Node:
Lactic acidosis (HP:0003128)

..Starting node
..Persistent lactic acidosis (HP:0004898)

Term ID:

4898

Name:

Persistent lactic acidosis

Synonym:

Definition:

A continuous form of lactic acidemia.

Comments:

Reference:

HP:0004898

Genes and Diseases:

Child Nodes:

Sister Nodes:

Chronic lactic acidosis (HP:0004925)

Congenital lactic acidosis (HP:0004902)

Exercise-induced lactic acidemia (HP:0004901)

Intermittent lactic acidemia (HP:0004913)

Lacticaciduria (HP:0003648)

Severe lactic acidosis (HP:0004900)

Stress/infection-induced lactic acidosis (HP:0004897)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0004898	HP:0004898	Persistent lactic acidosis	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.