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 branched chain amino acid concentration (HP:0010892)

Parent Node:
Abnormal circulating valine concentration (HP:0010914)

..Starting node
..Hypervalinemia (HP:0010910)

Term ID:

10910

Name:

Hypervalinemia

Synonym:

High blood valine concentration

Definition:

An increased concentration of valine in the blood.

Comments:

Reference:

HP:0010910

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010910	HP:0010910	Hypervalinemia	0	BCAT2 CL E G H	587	977	OMIM:618850	HYPERVALINEMIA AND HYPERLEUCINE-ISOLEUCINEMIA; HVLI
HP:0010910	HP:0010910	Hypervalinemia	0	MICU1 CL E G H	10367	1530	OMIM:615673	Myopathy with extrapyramidal signs	14

Genes (2) :BCAT2 MICU1

Diseases (2) :OMIM:618850 OMIM:615673

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.