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 lymphatic vessel morphology (HP:0100766)

Parent Node:
Abnormal pancreas morphology (HP:0012090)

Parent Node:
Lymphangiectasis (HP:0031842)

..Starting node
..Pancreatic lymphangiectasis (HP:0006273)

Term ID:

6273

Name:

Pancreatic lymphangiectasis

Synonym:

Definition:

The presence of lymphangiectasis in the pancreas.

Comments:

Reference:

HP:0006273

Genes and Diseases:

Child Nodes:

Sister Nodes:

Intestinal lymphangiectasia (HP:0002593)

Pericardial lymphangiectasia (HP:0005183)

Pleural lymphangiectasia (HP:0006531)

Pulmonary lymphangiectasia (HP:0006521)

Thyroid lymphangiectasia (HP:0008229)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006273	HP:0006273	Pancreatic lymphangiectasis	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.