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:
Abnormality of prenatal development or birth (HP:0001197)

Parent Node:
Prenatal movement abnormality (HP:0001557)

..Starting node
..Increased fetal movement (HP:0010519)

Term ID:

10519

Name:

Increased fetal movement

Synonym:

Fetal hyperkinesia; Foetal hyperkinesia; Increased foetal movement

Definition:

An abnormal increase in quantity or strength of fetal movements.

Comments:

Reference:

HP:0010519

Genes and Diseases:

Child Nodes:

Sister Nodes:

Decreased fetal movement (HP:0001558)

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:0010519	HP:0010519	Increased fetal movement	0	GLRB CL E G H	2743	4329	OMIM:614619	Hyperekplexia 2	46
HP:0010519	HP:0010519	Increased fetal movement	0	NEXMIF CL E G H	340533	29433	OMIM:300912	Mental retardation, X-linked 98	52

Genes (2) :GLRB NEXMIF

Diseases (2) :OMIM:614619 OMIM:300912

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