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:
Intracranial hemorrhage (HP:0002170)

Parent Node:
Intraventricular hemorrhage (HP:0030746)

..Starting node
..Preterm intraventricular hemorrhage (HP:0030747)

Term ID:

30747

Name:

Preterm intraventricular hemorrhage

Synonym:

Preterm intraventricular haemorrhage

Definition:

Intraventricular hemorrhage that occurs in a premature infant.

Comments:

Reference:

HP:0030747

Genes and Diseases:

Child Nodes:

........

Grade I preterm intraventricular hemorrhage (HP:0030748)

........

Grade II preterm intraventricular hemorrhage (HP:0030749)

........

Grade III preterm intraventricular hemorrhage (HP:0030750)

........

Grade IV preterm intraventricular hemorrhage (HP:0030751)

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030747	HP:0030747	Preterm intraventricular hemorrhage	0	CL E G H
HP:0030747	HP:0030749	Grade II preterm intraventricular hemorrhage	1	CL E G H
HP:0030747	HP:0030748	Grade I preterm intraventricular hemorrhage	1	CL E G H
HP:0030747	HP:0030751	Grade IV preterm intraventricular hemorrhage	1	CL E G H
HP:0030747	HP:0030750	Grade III preterm intraventricular hemorrhage	1	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.