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:
Abnormality of coagulation (HP:0001928)

Parent Node:
Abnormality of fibrinolysis (HP:0040224)

..Starting node
..Hyperfibrinolysis (HP:0040236)

Term ID:

40236

Name:

Hyperfibrinolysis

Synonym:

Definition:

Increased degradation of fibrin, associated with clot instability and bleeding

Comments:

Reference:

HP:0040236

Genes and Diseases:

Child Nodes:

Sister Nodes:

Prolonged euglobulin clot lysis time (HP:0040243)

Reduced euglobulin clot lysis time (HP:0040247)

Reduced plasminogen activator inhibitor 1 activity (HP:0040248)

Reduced plasminogen activator inhibitor 1 antigen (HP:0040249)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040236	HP:0040236	Hyperfibrinolysis	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.