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

..Starting node
..Splenic infarction (HP:0034336)

Term ID:

34336

Name:

Splenic infarction

Synonym:

Spleen infarct; Spleen infarction; Splenic infarct

Definition:

Ischemia and necrosis of part or all of the spleen resulting from compromise of blood supply resulting from arterial or venous occlusion.

Comments:

Reference:

HP:0034336

Genes and Diseases:

Child Nodes:

Sister Nodes:

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:0034336	HP:0034336	Splenic infarction	0	HBB CL E G H	3043	4827	OMIM:603903	Sickle cell anemia	580

Genes (1) :HBB

Diseases (1) :OMIM:603903

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