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 corpus striatum morphology (HP:0010994)

Parent Node:
Abnormal caudate nucleus morphology (HP:0002339)

..Starting node
..Increased caudate lactate level (HP:0012644)

Term ID:

12644

Name:

Increased caudate lactate level

Synonym:

Definition:

An elevated concentration of lactate in the caudate nucleus. This finding can be elicited by magnetic resonance spectroscopy imaging.

Comments:

Reference:

HP:0012644

Genes and Diseases:

Child Nodes:

Sister Nodes:

Atrophy/Degeneration involving the caudate nucleus (HP:0007374)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012644	HP:0012644	Increased caudate lactate level	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.