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:
Abnormal platelet count (HP:0011873)

Parent Node:
Thrombocytopenia (HP:0001873)

..Starting node
..Heparin-induced thrombocytopenia (HP:0011874)

Term ID:

11874

Name:

Heparin-induced thrombocytopenia

Synonym:

Definition:

Low platelet count following administration of unfractionated or (less commonly) low-molecular weight heparin.

Comments:

Reference:

HP:0011874

Genes and Diseases:

Child Nodes:

Sister Nodes:

Amegakaryocytic thrombocytopenia (HP:0004859)

Autoimmune thrombocytopenia (HP:0001973)

Congenital thrombocytopenia (HP:0001905)

Intermittent thrombocytopenia (HP:0004854)

Macrothrombocytopenia (HP:0040185)

Neonatal alloimmune thrombocytopenia (HP:0004809)

Post-transfusion thrombocytopenia (HP:0004813)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011874	HP:0011874	Heparin-induced thrombocytopenia	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.