Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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 heart morphology (HP:0001627)

Parent Node:
Abnormal cardiac atrium morphology (HP:0005120)

..Starting node
..Atrial septal hypertrophy (HP:0031296)

Term ID:

31296

Name:

Atrial septal hypertrophy

Synonym:

Definition:

An abnormal increase in the thickness of the atrial septum.

Comments:

Reference:

HP:0031296

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal atrial arrangement (HP:0011535)

Abnormal coronary sinus morphology (HP:0011642)

Abnormal left atrium morphology (HP:0025579)

Abnormal right atrium morphology (HP:0025580)

Atrial septal defect (HP:0001631)

Common atrium (HP:0011565)

Cor triatriatum (HP:0010774)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031296	HP:0031296	Atrial septal hypertrophy	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.