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:
Dilatation of an abdominal artery (HP:0002636)

Parent Node:
Dilatation of mesenteric artery (HP:0011934)

..Starting node
..Dilatation of Inferior mesenteric artery (HP:0100860)

Term ID:

100860

Name:

Dilatation of Inferior mesenteric artery

Synonym:

Inferior mesenteric artery aneurysm

Definition:

Abnormal outpouching or sac-like dilatation in the wall of the inferior mesenteric artery .

Comments:

Reference:

HP:0100860

Genes and Diseases:

Child Nodes:

Sister Nodes:

Dilatation of superior mesenteric artery (HP:0100859)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100860	HP:0100860	Dilatation of Inferior mesenteric artery	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.