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 cardiac ventricle morphology (HP:0001713)

Parent Node:
Single ventricle (HP:0001750)

..Starting node
..Single ventricle of indeterminate morphology (HP:0011680)

Term ID:

11680

Name:

Single ventricle of indeterminate morphology

Synonym:

Definition:

Comments:

Reference:

HP:0011680

Genes and Diseases:

Child Nodes:

Sister Nodes:

Double inlet left ventricle (HP:0011555)

Double inlet right ventricle (HP:0011556)

Double inlet to single ventricle of indeterminate morphology (HP:0011557)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011680	HP:0011680	Single ventricle of indeterminate morphology	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.