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 coronary artery morphology (HP:0006704)

Grandparent Node:
Arterial stenosis (HP:0100545)

Grandparent Node:
Atherosclerosis (HP:0002621)

Parent Node:
Coronary artery atherosclerosis (HP:0001677)

..Starting node
..Post-angioplasty coronary artery restenosis (HP:0004761)

Term ID:

4761

Name:

Post-angioplasty coronary artery restenosis

Synonym:

Definition:

Comments:

Reference:

HP:0004761

Genes and Diseases:

Child Nodes:

Sister Nodes:

Nonocclusive coronary artery atherosclerosis (HP:0012436)

Premature coronary artery atherosclerosis (HP:0005181)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0004761	HP:0004761	Post-angioplasty coronary artery restenosis	0	SERPIND1 CL E G H	3053	4838	OMIM:612356	Heparin cofactor II deficiency	.	5

Genes (1) :SERPIND1

Diseases (1) :OMIM:612356

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