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 lung morphology (HP:0002088)

Parent Node:
Abnormal lung lobation (HP:0002101)

..Starting node
..Bilateral trilobed lung (HP:0011861)

Term ID:

11861

Name:

Bilateral trilobed lung

Synonym:

Bilateral trilobed lungs

Definition:

Both lungs have three lobes. Normally, the left lung has two lobes, whereas the right lung has three lobes.

Comments:

Reference:

HP:0011861

Genes and Diseases:

Child Nodes:

Sister Nodes:

Pulmonary sequestration (HP:0100632)

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:0011861	HP:0011861	Bilateral trilobed lung	0	CHUK CL E G H	1147	1974	OMIM:613630	Fetal encasement syndrome	3
HP:0011861	HP:0011861	Bilateral trilobed lung	0	NODAL CL E G H	4838	7865	OMIM:270100	Heterotaxy, visceral, 5	45
HP:0011861	HP:0011861	Bilateral trilobed lung	0	ZIC3 CL E G H	7547	12874	OMIM:306955	Heterotaxy, visceral, 1, X-linked	39

Genes (3) :CHUK NODAL ZIC3

Diseases (3) :OMIM:613630 OMIM:270100 OMIM:306955

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