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 CSF metabolite concentration (HP:0025454)

Parent Node:
Abnormal CSF lactate concentration (HP:0030085)

..Starting node
..Reduced CSF lactate (HP:0030086)

Term ID:

30086

Name:

Reduced CSF lactate

Synonym:

Hypolactatorachia

Definition:

Decreased concentration of lactate in the cerebrospinal fluid.

Comments:

Reference:

HP:0030086

Genes and Diseases:

Child Nodes:

Sister Nodes:

Increased CSF lactate (HP:0002490)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030086	HP:0030086	Reduced CSF lactate	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.