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 carboxylic acid concentration (HP:0004354)

Parent Node:
Abnormal circulating monocarboxylic acid concentration (HP:0010996)

..Starting node
..Increased level of myristic acid in serum (HP:0410154)

Term ID:

410154

Name:

Increased level of myristic acid in serum

Synonym:

Increased level of tetradecanoic acid in serum

Definition:

An increase in the level of myristic acid in the serum.

Comments:

Reference:

HP:0410154

Genes and Diseases:

Child Nodes:

Sister Nodes:

4-hydroxyphenylacetic aciduria (HP:0003607)

4-Hydroxyphenylpyruvic aciduria (HP:0003161)

Abnormal serum bile acid concentration (HP:0030984)

obsolete Increased urinary orotic acid concentration (HP:0010928)

Reduced 4-Hydroxyphenylpyruvate dioxygenase level (HP:0003637)

Urocanic aciduria (HP:0012237)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0410154	HP:0410154	Increased level of myristic acid in serum	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.