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:
Congenital malformation of the great arteries (HP:0011603)

Parent Node:
Patent ductus arteriosus (HP:0001643)

..Starting node
..Patent ductus arteriosus after premature birth (HP:0011649)

Term ID:

11649

Name:

Patent ductus arteriosus after premature birth

Synonym:

Definition:

Abnormal persistent patency of the ductus arteriosus when birth was at less than 37 weeks completed gestation.

Comments:

Reference:

HP:0011649

Genes and Diseases:

Child Nodes:

Sister Nodes:

Bilateral ductus arteriosus (HP:0011650)

Patent ductus arteriosus after birth at term (HP:0011648)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011649	HP:0011649	Patent ductus arteriosus after premature birth	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.